Focused libraries of genetic packages

ABSTRACT

Focused libraries of vectors or genetic packages that display, display and express, or comprise a member of a diverse family of antibody peptides, polypeptides or proteins and collectively display, display and express, or comprise at least a portion of the focused diversity of the family. The libraries have length and sequence diversities that mimic that found in native human antibodies.

This application is a continuation of U.S. application Ser. No.12/762,051, filed on Apr. 16, 2010, now published, which is acontinuation of U.S. application Ser. No. 11/416,460, filed on May 1,2006, now abandoned, which is a continuation of U.S. application Ser.No. 10/026,925, filed on Dec. 18, 2001, now abandoned, which claims thebenefit under 35 USC §120 of U.S. provisional application 60/256,380,filed Dec. 18, 2000 the entire content of each of which is hereinincorporated by reference. The provisional application and the Tablesattached to it are specifically incorporated by reference herein.

The present invention relates to focused libraries of genetic packagesthat each display, display and express, or comprise a member of adiverse family of peptides, polypeptides or proteins and collectivelydisplay, display and express, or comprise at least a portion of thefocused diversity of the family. The focused diversity of the librariesof this invention comprises both sequence diversity and lengthdiversity. In a preferred embodiment, the focused diversity of thelibraries of this invention is biased toward the natural diversity ofthe selected family. In more preferred embodiment, the libraries arebiased toward the natural diversity of human antibodies and arecharacterized by variegation in their heavy chain and light chaincomplementarity determining regions (“CDRs”).

The present invention further relates to vectors and genetic packages(e.g., cells, spores or viruses) for displaying, or displaying andexpressing a focused diverse family of peptides, polypeptides orproteins. In a preferred embodiment the genetic packages are filamentousphage or phagemids or yeast. Again, the focused diversity of the familycomprises diversity in sequence and diversity in length.

The present invention further relates to methods of screening thefocused libraries of the invention and to the peptides, polypeptides andproteins identified by such screening.

BACKGROUND OF THE INVENTION

It is now common practice in the art to prepare libraries of geneticpackages that individually display, display and express, or comprise amember of a diverse family of peptides, polypeptides or proteins andcollectively display, display and express, or comprise at least aportion of the amino acid diversity of the family. In many commonlibraries, the peptides, polypeptides or proteins are related toantibodies (e.g., single chain Fv (scFv), Fv, Fab, whole antibodies orminibodies (i.e., dimers that consist of V_(H) linked to V_(L))). Often,they comprise one or more of the CDRs and framework regions of the heavyand light chains of human antibodies.

Peptide, polypeptide or protein libraries have been produced in severalways in the prior art. See e.g., Knappik et al., J. Mol. Biol., 296, pp.57-86 (20004, which is incorporated herein by references. One method isto capture the diversity of native donors, either naive or immunized.Another way is to generate libraries having synthetic diversity. A thirdmethod is combination of the first two. Typically, the diversityproduced by these methods is limited to sequence diversity, i.e., eachmember of the library differs from the other members of the family byhaving different amino acids or variegation at a given position in thepeptide, polypeptide or protein chain. Naturally diverse peptides,polypeptides or proteins, however, are not limited to diversity only intheir amino acid sequences. For example, human antibodies are notlimited to sequence diversity in their amino acids, they are alsodiverse in the lengths of their amino acid chains.

For antibodies, diversity in length occurs, for example, during variableregion rearrangements. See e.g., Corbett et al., J. Mol. Biol., 270, pp.587-97 (1997). The joining of V genes to J genes, for example, resultsin the inclusion of a recognizable D segment in CDR3 in about half ofthe heavy chain antibody sequences, thus creating regions encodingvarying lengths of amino-acids. The following also may occur duringjoining of antibody gene segments: (i) the end of the V gene may havezero to several base deleted or changed; (ii) the end of the D segmentmay have zero to many bases removed or changed; (iii) a number of randombases may be inserted between V and D or between D and J; and (iv) the5′ end of J may be edited to remove or to change several bases. Theserearrangements result in antibodies that are diverse both in amino acidsequence and in length.

Libraries that contain only amino acid sequence diversity are, thusdisadvantaged in that they do not reflect the natural diversity of thepeptide, polypeptide or protein that the library is intended to mimic.Further, diversity in length may be important to the ultimatefunctioning of the protein, peptide or polypeptide. For example, withregard to a library comprising antibody regions, many of the peptides,polypeptides, proteins displayed, displayed and expressed, or comprisedby the genetic packages of the library may not fold properly or theirbinding to an antigen may be disadvantaged, if diversity both insequence and length are not represented in the library.

An additional disadvantage of prior art libraries of genetic packagesthat display, display and express, or comprise peptides, polypeptidesand proteins is that they are not focused on those members that arebased on natural occurring diversity and thus on members that are mostlikely to be functional. Rather, the prior art libraries, typically,attempt to include as much diversity or variegation at every amino acidresidue as possible. This makes library construction time-consuming andless efficient than possible. The large number of members that areproduced by trying to capture complete diversity also makes screeningmore cumbersome than it needs to be This is particularly true given thatmany members of the library will not be functional.

SUMMARY OF THE INVENTION

One objective of this invention is focused libraries of vectors orgenetic packages that encode members of a diverse family of peptides,polypeptides or proteins wherein the libraries encode populations thatare diverse in both length and sequence. The diverse length comprisingcomponents contain motifs that are likely to fold and function in thecontext of the parental peptide, polypeptide or protein.

Another object of this invention is focused libraries of geneticpackages that display, display and express, or comprise a member of adiverse family of peptides, polypeptides and proteins and collectivelydisplay, display and express, or comprise at least a portion of thefocused diversity of the family. These libraries are diverse not only intheir amino acid sequences, but also in their lengths. And, theirdiversity is focused so as to more closely mimic or take into accountthe naturally-occurring diversity of the specific family that thelibrary represents.

Another object of this invention is diverse, but focused, populations ofDNA sequences encoding peptides, polypeptides or proteins suitable fordisplay or display and expression using genetic packages (such as phageor phagemids) or other regimens that allow selection of specific bindingcomponents of a library.

A further object of this invention is focused libraries comprising theCDRs of human antibodies that are diverse in both their amino acidsequence and in their length (examples of such libraries includelibraries of single chain Fv(scFv), Fv, Fab, whole antibodies orminibodies (i.e., dimers that consist of V_(H) linked to V_(L)). Suchregions may be from the heavy or light chains or both and may includeone or, more of the CDRs of those chains. More preferably, theydiversity or variegation occurs in all of the heavy chain and lightchain CDRs.

It is another object of this invention to provide methods of making andscreening the above libraries and the peptides, polypeptides andproteins obtained in such screening.

Among the preferred embodiments of this invention are the following:

1. A focused library of vectors or genetic packages that display,display and express, or comprise a member of a diverse family of humanantibody related peptides, polypeptides and proteins and collectivelydisplay, display and express, or comprise at least a portion of thediversity of the antibody family, the vectors or genetic packages beingcharacterized by variegated DNA sequences that encode a heavy chain CDR1selected from the group consisting of:

-   -   (1) <1>₁Y₂<1>₃M₄<1>₅ (SEQ ID NO:100), wherein <1> is an        equimolar mixture of each of amino acid residues A, D, E, F, G,        H, I, K, L, M, N, P, Q, R, S, T, V, W, and Y;    -   (2) (S/T)₁(S/G/X)₂(S/G/X)₃Y₄Y₅W₆(S/G/X)₇ (SEQ ID NO:101) wherein        (S/T) is a 1:1 mixture of S and T residues, (S/G/X) is a mixture        of 0.2025 S, 0.2025 G and 0.035 of each of amino acid residues        A, D, E, F, H, I, K, L, H, N, P, Q, R, T, V, W, and Y;    -   (3) V₁S₂G₃G₄S₅I₆S₇<1>₈<1>₉<1>₁₀Y₁₁Y₁₂W₁₃<1>₁₄ (SEQ ID NO:1),        wherein <1> is an equimolar mixture of each of amino acid        residues A, D, E, F, G, H, I, K, L, M, N, P, Q, R, S, T, V, W,        and Y; and    -   (4) mixtures of vectors or genetic packages characterized by any        of the above DNA sequences, preferably in the ratio: HC CDR1s        (1):(2):(3)::0.80:0.17:0.02.

2. A focused library of vectors or genetic packages that display,display and express, or comprise a member of a diverse family of humanantibody related peptides, polypeptides and proteins and collectivelydisplay, display and express or comprise at least a portion of thediversity of the antibody facility, the vectors or genetic packagesbeing characterized by variegated DNA sequences that encode a heavychain CDR2 selected from the group consisting of:

-   -   (1) <2>I<2><3>SGG<1>T<1>YADSVKG (SEQ ID NO:2), wherein <1> is an        equimolar mixture of each of amino acid residues 2¹1, 0, E, F,        G, H, I, K, L, M, N, P, 0, P, S, T, V, W, and Y; <2> is an        equimolar mixture of each of amino acid residues Y, R, W, V, G,        and S; and <3> is an equimolar mixture of each of amino acid        residues P, S, and G or an equimolar mixture of P and S;    -   (2) <1>I<4><1><1><G><5><1><1><1>YADSVKG (SEQ ID NO:3), wherein        <1> is an equimolar mixture of each of amino acid residues A, D,        E, F, G, H, I, K, L, M, N, P, Q, R, S, T, V, W, and Y; <4> is an        equimolar mixture of residues D, I, N, S, W, Y; and <5> is an        equimolar mixture of residues S, G, D and N;    -   (3) <1>I<4><1><1>G<5><1><1>YNPSLKG (SEQ ID NO:4), wherein <1> is        an equimolar mixture of each of amino acid residues A, D, E, F,        G, H, I, K, L, M, N; P, Q, R, S, T, V, W and Y, and <4> and <5>        are as defined above;

(4) <1>I<8>S<1><1><1>GGYY<1>YAASVKG (SEQ ID NO:5), wherein <1> is anequimolar mixture of each amino acid residues A, D, E, F, Gill, I, K, L,M, N, P, Q, R, S, T, V, and Y; <8> is 0.27 R and 0.027 of each ofADEFGHIKLMNPQSTVWY; and

-   -   (5) mixtures of vectors or genetic packages characterized by any        of the above DNA sequences, preferably in the ratio: HC CDR2s:        (1)/(2) (equimolar): (3):(4)::0.54:0.43:0.03.

3. A focused library of vectors or genetic packages that display,display and express, or comprise a member of a diverse family of humanantibody related peptides, polypeptides and proteins and collectivelydisplay, display and express, or comprise at least a portion of thediversity of the antibody family, the vectors or genetic packages beingcharacterized by variegated DNA sequences that encode a heavy chain CDR3was selected from the group consisting of:

-   -   (1) YYCA21111YFDYWG (SEQ ID NO:6), Wherein 1 is an equimolar        mixture of each amino acid residues A, D, E, F, G, H, I, K, L,        M, N, P, Q, R, S, T, V, W and Y; and 2 is an equimolar mixture        of K and R;    -   (2) YYCA2111111YFDYWG (SEQ ID NO:7), wherein 1 is an equimolar        mixture of each amino acid residues A, D, E, F, G, H, K, L, M,        N, P, Q, R, S, T, V, W and Y; and 2 is an equimolar mixture of K        and R;    -   (3) YYCA211111111YFDAYTG (SEQ ID NO:8), wherein 1 is an        equimolar mixture of each amino acid residues A, D, E, F, G, H,        1, K, L, M, N, P, Q, R, S, T, V, W and Y; and 2 is an equimolar        mixture of K and R;    -   (4) YYCAR111S2S3111YFDYWG (SEQ ID NO:9), wherein 1 is an        equimolar mixture of each amino acid residues A, D, E, G, H, I,        K, L, M, N, P, Q, R, S, T, V, W and Y; and 2 is an equimolar        mixture of S and G; and 3 is an equimolar mixture of Y and W;    -   (5) YYCA2111CSG11CY1YFDYWG (SEQ ID NO:10), wherein 1 is an        equimolar mixture of each amino acid residues A, D, E, F, G, H,        I, K, L, M, N, P, Q, R, S, T, V, W and Y; and 2 is an equimolar        mixture of K and R;    -   (6) YYCA211S1TIFG11111YFDYWG (SEQ ID NO:11), wherein 1 is an        equimolar mixture of each amino acid residues A, D, E, F, G, H,        I, K, L, M, N, P, Q, R, S, T, V, W and Y; and 2 is an equimolar        mixture of K and R.    -   (7) YYCAR111YY2S3344111YFDYWG (SEQ ID NO:12), wherein 1 is an        equimolar mixture of each amino acid residues A, D, E, F, G, H,        I, K, L, M, N, P, Q, R, S, T, V, W and Y; 2 is an equimolar        mixture of D and S; and 3 is an equimolar mixture of S and G;    -   (8) YYCAR1111YC2231CY111YFDYWG (SEQ ID NO:13), wherein 1 is an        equimolar mixture of each amino acid residues A, D, E, F, G, H,        I, K, L, M, N, P, Q, R, S, T, V, W and Y; 2 is an equimolar        mixture of S and G; and 3 is an equimolar mixture of T, D and G;        and    -   (9) mixtures of vectors or genetic packages characterized by any        of the above DNA sequences, preferably the HC CDR3s (1)        through (8) are in the following proportions in the mixture:

(1) 0.10

(2) 0.14

(3) 0.25

(4) 0.13

-   -   (5) 0.13

(6) 0.11

(7) 0.04 and

(8) 0.10; and more preferably the HC CDR3s (1) through (8) are in thefollowing proportions in the mixture:

(1) 0.02

(2) 0.14

(3) 0.25

(4) 0.14

-   -   (5) 0.14    -   (6) 0.12    -   (7) 0.08 and    -   (8) 0.11.

Preferably, 1 in one or all of HC CDR3s (1) through (8) is 0.095 of eachof G and Y and 0.048 of each of A, D, E, F H, 1, K, L, M, N, P, Q, R, S,T, V, and W.

4. A focused library of vectors or genetic packages that display,display and express, or comprise a member of a diverse family of humanantibody related peptides, polypeptides and proteins and collectivelydisplay, display and express, or comprise at least a portion of thediversity of the antibody family, the vectors or genetic packages beingcharacterized by variegated DNA sequences that encodes a kappa lightchain CDR1 selected from the group consisting of:

(1) RASQ<1>V<2><2><3>LA (SEQ ID NO:14)

(2) RASQ<1>V<2><2><2><3>LA (SEQ ID NO:15); wherein <1> is an equimolarmixture of amino acid residues ADEFGHIKLMNPQRSTVWY; <2> is 0.2 S and0.044 of each of ADEFGHIKLMNPQRTVWY; and <3> is 0.2Y and 0.044 each ofADEFGHIKLMNPQRTVW and S; and

(3) mixtures of vectors or genetic packages characterized by any of theabove DNA sequences, preferably in the ratio CDR1s (1):(2)::0.68:0.32.

5. A focused library of vectors or genetic packages that display,display and express, or comprise a member of a diverse family of humanantibody related peptides, polypeptides and proteins and collectivelydisplay, display and express, or comprise at least a portion of thediversity of the-antibody family the vectors or genetic packages beingcharacterized by variegated DNA sequences that encode a kappalight-chain CDR2 having the sequence:

-   -   <1>AS<2>R<4><1> (SEQ ID NO:102), wherein <1> is an equimolar        mixture of amino acid residues ADEFGHIKLMNPQRSTVWY; <2> is 0.2 S        and 0.044 of each of ADEFGHIKLMNPQRTVWY; and <4> is 0.2.A and        0.044 each of DEFGHIKLMNPQRSTVWY.

6. A focused library of vectors or genetic packages that display,display and express, or comprise a member of a diverse family of humanantibody related peptides, polypeptides and proteins and collectivelydisplay, display and express, or comprise at least a portion of thediversity of the antibody family, the vectors or genetic packages beingcharacterized by variegated DNA sequences that encode a kappa lightchain CDR3 selected from the groups consisting of:

-   -   (1) QQ<3><1><1><1>P<1>T (SEQ ID NO:16), wherein <1> is an        equimolar mixture of amino acid residues ADEFGHIKLMNPQRSTVWY;        <3> is 0.2 Y and 0.044 each of ADEFGHIKIMNPQRTVW;    -   (2) QQ33111P (SEQ ID NO:103), wherein 1 and 3 are as defined        in (1) above;    -   (3) QQ3211PP1T (SEQ ID NO:17), wherein 1 and 3 are as defined        in (1) above and 2 is 0.2 S and 0.044 each of        ADEFGHIKLMNPQRTVWY; and    -   (4) mixtures of vectors or genetic packages characterized by any        of the above DNA sequences, preferably in the ratio CDA3s        (1):(2):(3)::0.65:0.1:0.25.

7. A focused library of vectors or genetic packages that display,display and express, or comprise a member of a diverse family of humanantibody related peptides, polypeptides and proteins and collectivelydisplay, display and express, or comprise at least a portion of thediversity of the antibody family, the vectors or genetic packages beingcharacterized by variegated DNA sequences that encode a lambda lightchain CDR1 selected from the group consisting of:

-   -   (1) TG<1>SS<2>VG<1><3><2><3>VS (SEQ ID NO:18), wherein <1> is        0.27 T, 0.27 G and 0.027 each of ADEFRIKLMNPQRSVWY: <2> is 0.27        D, 0.27 N and 0.027 each of AEFGHIKLMPQRSTVWY, and <3> is 0.36 Y        and 0.036 each of ADEFGHIKLMNPQRSTVW;    -   (2) G<2><4>L<4><4><4><3><4><4> (SEQ ID NO:104), wherein <2> is        as defined in (1) above and <4> is an equimolar mixture of amino        acid residues ADEFGHIKIMNPQRSTVWY; and    -   (3) mixtures of vectors or genetic packages 5 characterized by        any of the above DNA sequences, preferably in the ratio CDR1        (1):(2)::0.67:0.33;

8. A focused library of vectors or genetic packages that display,display and express, or comprise a member of a diverse family of humanantibody related peptides, polypeptides and proteins and collectivelydisplay, display and express, or comprise at least a portion of thediversity of the antibody family, the vectors or genetic packages beingcharacterized by variegated DNA sequences that encode a lambda lightchain CDR2 has the sequence:

-   -   <4><4><4><2>RPS (SEQ ID NO:105) wherein <2> is 0.27 D, 0.27 N,        and 0.027 each of AEFGHIKIMPQRSTVWY and <4> is an equimolar        mixture of amino acid residues ADEFGHIKLONPQRSTVW.

9. A focused library of vectors or genetic packages that display,display and express, or comprise a member of a diverse family of humanantibody related peptides, polypeptides and proteins and collectivelydisplay, display and express, or comprise at least a portion of thediversity of the antibody family, the vectors or genetic packages beingcharacterized by variegated DNA sequences that encode a lambda lightchain CDR3 selected from the group consisting of:

-   -   (1) <4><5><4><2><4>S<4><4><4><4>V (SEQ ID NO:106), wherein <2>        is 0.27 D, 0.27 N, and 0.027 each of AEFGHIKIMPQRSTVWY; <4> is        an equimolar mixture of amino acid residues ADEFGHIKLMVPQRSTVW;        and <5> is 0.36 S and 0.6355 each of ADEFGHIKLMNPQRTVWY;

(2) <5>SY<1><5>S<5><1><4>V (SEQ ID NO:19), wherein <1> is an equimolarmixture of ADEFGHIKLMNPQRSTVWY; and <4> and 5 <5> are as defined in (1)above; and

-   -   (3) mixtures of vectors or genetic packages characterized by any        of the above DNA sequences, preferably in the ratio CDR3s

10. A focused library comprising variegated-DNA sequences that encode aheavy chain CDR selected from the group consisting of:

-   -   (1) one or more of the heavy chain CDR's of paragraph 1 above;    -   (2) one or more of the heavy chin CDR2s of paragraph 2 above;    -   (3) one or more of the heavy chain CDR3s of paragraph 3 above;        and    -   (4) mixtures of vectors or genetic-packages characterized by        (1), (2) and (3).

11. The focused library comprising one or more of the variegated DNAsequences that encodes a heavy chain CDR of paragraphs 1, 2 and 3 andfurther comprising variegated DNA sequences that encodes a light chainCDR selected from the group consisting of

-   -   (1) one or more the kappa light chain CDR1s of paragraph 4;    -   (2) the kappa light chain. CDR2 of paragraph 5;    -   (3) one or more of the kappa light chain CDR3s of paragraph 6;    -   (4) one or more of the kappa light chain CDR1s of paragraph 7;    -   (5) the lambda light chain ‘CDR2’ of paragraph 8    -   (6) one or more of the lambda light chain CDR3s of paragraph. 9;        and    -   (7) mixtures of vectors and genetic packages characterized by        one or more of (1) through (6).

12. A population of variegated DNA sequences as. described in paragraphs1-11 above.

13. A population of vectors comprising the variegated DNA sequences asdescribed in paragraphs 1-11 above.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

Antibodies (“Ab”) concentrate their diversity into those regions thatare involved in determining affinity and specificity of the Ab forparticular targets. These regions may be diverse in sequence or inlength. Generally, they are diverse In both ways. However, withinfamilies of human antibodies the diversities, both in sequence and inlength, are not truly random. Rather, some amino acid residues arepreferred at certain positions of the CDRs and some CDR lengths arepreferred. These preferred diversities account for the natural diversityof the antibody family.

According to this invention, and as more fully described below,libraries of vectors and genetic packages that more closely mirror thenatural diversity, both in sequence and in length, of antibody families,or portions thereof are prepared and used.

Human Antibody Heavy Chain Sequence and Length Diversity

(a) Framework

The heavy chain (“HC”) Germ-Line Gene (GLG) 3-23 (also known as 1/1)-47)accounts for about 12% of all human Abs and is preferred as theframework in the preferred embodiment of the invention. It should,however, be understood that other well-known frameworks, such as 4-34,3-30, 3-30.3 and 4-30.1, may also be used without departing from theprinciples of the focused diversities of this invention.

In addition, JH4(YFDYWGQGTLVTVSS; SEQ ID NO:20) occurs more often thanJH3 in native antibodies. Hence, it is preferred for the focusedlibraries of this invention. However, JH3 (AFDIWGQGTMVTVSS; SEQ IDNO:21) could as well be used.

(b) Focused Length Diversity: CDR1, 2 and 3

(i) CDR1

For CDR1, GLGs provide CDR1s only Of the lengths 5, 6, and 7. Mutationsduring the maturation of the v-domain gene, however, can lead to CDR1shaving lengths as short as 2 and as long as 16. Nevertheless, length 5,predominates. Accordingly, in the preferred embodiment of this inventionthe preferred HC CDR1 is 5 amino acids, with less preferred CDR1s havinglengths of 7 and 14. In the most preferred libraries of this invention,all three lengths are used in proportions similar to those found innatural antibodies.

(ii) CDR2

GLGs provide CDR2s only of the lengths 15:19, but mutations duringmaturation may result in CDR2s of lengths from 16 to 28 amino acids. Thelengths 16 and 17 predominate in mature Ab genes. Accordingly, length 17is the preferred length for HC CDR2 of the present invention. Lesspreferred HC CDR2s of this invention have lengths 16 and 19. In the mostpreferred focused libraries of this invention, all three lengths areincluded in proportions similar to those found in natural antibodyfamilies.

(iii) CDR3

HC CDR3s vary in length. About half of human HCs consist of thecomponents: V::nz::D::ny::JHn where V is a V gene, nz is a series ofbases (mean 12) that are essentially random, D is a D segment, oftenwith heavy editing at both ends, ny is a series of bases (mean 6) thatare essentially random, and JH is one of the six JH segments, often withheavy editing at the 5′ end. The D segments appear to provide spacersegments that allow folding of the IgG. The greatest diversity is at thejunctions of y with D and of D with JH.

In the preferred-libraries of this invention both types of HC CDR3s areused. In HC CDR3s that have no identifiable D segment, the structure isV::nz::JHn where JH is usually edited at the 5′ end. In HC CDR3s thathave an identifiable D segment, the structure is V::nz::D::ny::JHn.

(c) Focused Sequence Diversity: CDR1, 2 and 3

(i) CDR1

In 5 amino acid length CDR1, examination of a 3D model of a humanized Abshowed that the side groups of residues 1, 3, and 5 were directed towardthe combining pocket. Consequently, in the focused libraries of thisinvention, each of these positions may be selected from any of thenative amino acid residues, except cysteine (“C”). Cysteine can formdisulfide bonds, which are an important component of the canonical Igfold. Having free thiol groups Could, thus, interfere with properfolding of the HC and could lead to problems in production ormanipulation of selected Abs. Thus, in the focused libraries of thisinvention cysteine is excluded from positions 1; 3 and 5 of thepreferred 5 amino acid CDR1s. The other 19 natural amino acids residuesmay be used at positions 1, 3 and 5. Preferably, each is present inequimolar ratios in the variegated libraries of this invention.

3D modeling also suggests that the side groups of residue 2 in a 5 aminoacid CDR1 are directed away from the combining pocket. Although thisposition shows substantial diversity, both in GLG and mature genes, inthe focused libraries of this invention this residue is preferably Tyr(Y) because it occurs in 681/820 mature antibody genes. However, any ofthe other native amino acid residues, except Cys (C), could also be usedat this position.

For position 4, there is also some diversity in GLG and mature antibodygenes. However, almost all mature genes have uncharged hydrophobic aminoacid residues: A, G, L, P, F, M, W, I, V, at this position. Inspectionof a 3D model also shows that the side group of residue 4 is packed intothe innards of the HC. Thus, in the preferred embodiment of thisinvention which uses framework 3-23, residue 4 is preferably Met becauseit Is likely to fit very well into the framework of 3-23. With otherframeworks, a similar fit consideration is used to assign residue 4.

Thus, the most preferred HC CDR1 of this invention consists of the aminoacid sequence <1>Y<I>M<1> where <1> can be any one of amino acidresidues: A, D, E, G, H, I, K, L, M, N, R, Q, S, T, V, W, Y. (not C),preferably present at each position in an equimolar amount. Thisdiversity is shown in the context of a framework 3-23:JH4 in Table 1. Ithas a diversity of 6859-fold.

The two less preferred HC CDR1s of this invention have length 7 andlength 14. For length 7, a preferred variegation is(S/T)₁(S/G/<1>)₂(S/G/<1>)₃Y₄Y₅W₆(S/G/<1>)₇ (SEQ ID NO:107); where (S/T)indicates an equimolar mixture of Ser and Thr codons; (S/G/<1>)indicates a mixture Of 0.2025 S, 0.2025 G, and 0.035 for each of A, D,E, F, H, I, K, L, M, N, P, Q, R, T, V, W, Y. This design gives apredominance of Ser and Gly at positions 2, 3, and 7, as occurs inmature HC genes. For length 14, a preferred variegation isVSGGSIS<1><1><1>YYW<1> (SEQ ID NO:108), where <1> is an equimolarmixture of the 19 native amino acid residues, except Cys (C).

The DNA that encodes these preferred HC CDR1s is preferably synthesizedusing trinucleotide building blocks so that each amino acid residue iipresent in essentially equimolar or other described amounts. Thepreferred codons for the <1> amino acid residues are gct, gat, gag, ttt,ggt, cat, att, aag, ctt, atg, aat, cct, cag, cgt, tct, act, gtt, tgg,and tat. Of course, other codons for the chosen amino acid residue couldalso be used.

The diversity oligonucleotide (ON) is preferably synthesized from BspEIto BstXI (as shown in Table 1) and can, therefore, be incorporatedeither by PCR synthesis using overlapping ONs or introduced by ligationof BspEI/BstXI-cut fragments. Table 2 shows the oligonucleotides thatembody the specified variegations of the preferred length 5 HC CDR1s ofthis invention. PCR using ON-R1V1vg, ON-R1top, and ON-R1bot gives adsDNA product of 73 base-pairs, cleavage with 14spEI and BstXI trims 11and 13 bases from the ends and provides cohesive ends that can beligated to similarly cut vector having the 3-23 domain shown in Table 1.Replacement of ON-R1V1vg with either ONR1V2vg or ONR1V3vg (see Table 2)allows synthesis of the two alternative diversity patterns—the 7 residuelength and the 14 residue length HC CDR1.

The more preferred libraries of this invention comprise the 3 preferredHC CDR1 length diversities. Most preferably, the 3 lengths should beincorporated in approximately the ratios in which they are observed inantibodies selected without reference to the length of the CDRs. Forexample, one sample of 1095 HC genes have the three lengths present inthe ratio: L=5:L=7:L=14::820:175:23::0.80:0.17:0.02. This is thepreferred ratio in accordance with this invention.

(ii) CDR2

Diversity in HC CDR2 was designed with the same considerations as for HCCORI: GLG sequences, mature sequences and 3D structure. A preferredlength for CDR2 is 17, as shown in Table 1. For this preferred 17 lengthCDR2, the preferred variegation in accordance with the invention is:<2>I<2><3>SGG<1>T<1>YADSVKG (SEQ ID NO:2), where <2> indicates any aminoacid residue selected from the group of Y, R, W, V, G and S (equimolarmixture), <3> is P, S and G or P and S only (equimolar mixture), and <1>is any native amino acid residue except C (equimolar mixture).

ON-R2V1vg shown in Table 3 embodies this diversity pattern. It ispreferably synthesized so that fragments of dsDNA containing the BstXIand XbaI site can be generated by PCR. PCR with ON-R2V1vg, ON-R2top, andONR2bot gives a dsDNA product of 122 base pairs. Cleavage with BstXI andXbaI removes about 10 bases from each end and produces cohesive endsthat can be ligated to similarly cut vector that contains the 3-23gene-shown in Table 1.

In an alternative embodiment for a 17 length HC CDR2, the followingvariegation may be used; <1>I<4><1><1>G<5><1><1><1>YADSVKG (SEQ IDNO:3), where <1> is as described above for the more preferredalternative of HC CDR2; <4> indicates an equimolar mixture of DINSWY,and <5> indicates an equimolar mixture of SGDN. This diversity patternis embodied in ON-R2V2vg shown in Table 3. Preferably, the twoembodiments are used in equimolar mixtures in the libraries of thisinvention.

Other preferred HC CDR2s have lengths 16 and 19.

(SEQ ID NO: 4) Length 16: <1>I<4><1><1>G<5<1><1>YNPSLKG; (SEQ ID NO: 5)Length: 19: <1>I<8>S<1><1><1>GGYY<1>YAASVKG,wherein <1> is an equimolar mixture of all native amino acid residuesexcept C; <4> is a equimolar mixture of DINSWY; <5> is an equimolarmixture of SGDN; and <8> is 0.27 R and 0:0 7 of each of residuesADEFGHIKLMNPQSTVWY. Table 3 shows ON-R2V3vg which embodies a preferredaDR2 variegation of length 16 and ON7R2V4vg which embodies a preferredCDR2 variegation of length 19. To prepare these variegations ON-R2V3vgmay be PCR amplified with ON-A2top and ON-R2bo3 and ON-R2V4vg may be PCRamplified with ON-R2top and ON-R2-bo4. See Table 3. In the mostpreferred embodiment of this invention, all three HC CDR2 lengths areused. Preferably, they are present in a ratio17:16:19::579:464:31::0.54:0.43:0.03.

(iii) CDR3

The preferred libraries of this invention comprise several BC CDR3components. Some of these will have only sequence diversity. Others willhave sequence diversity with embedded D segments to extend the length,while also incorporating sequences known to allow Igs to fold. The HCCDR3 components of the preferred libraries of this invention and theirdiversities are depicted in Table 4: Components 1-8.

This set of components was chosen after studying the sequences of 1383human BC sequences. The proposed components are meant to fulfill thefollowing goals:

1) approximately the same distribution of lengths as seen in native Abgenes;

2) high level of sequence diversity at places having high diversity innative Ab genes; and

3) incorporation of constant sequences often seen in native Ab genes.

Component 1 represents all the genes having lengths 0 to 8 (countingfrom the YYCAR motif at the end of FR3 to the WG dipeptide motif nearthe start of the J region, i.e., FR4). Component 2 corresponds the allthe genes having lengths 9 or 10. Component 3.corresponds to the geneshaving lengths 11 or 12 plus half the genes having length 13. Component4 corresponds to those having length 14 plus half those having length13. Component 5 corresponds to the genes having length 15 and half ofthose having length 16. Component. 6 corresponds to genes of length 17plus half of those with length 16. Component 7 corresponds to those withlength 18. Component 8 corresponds to those having length 19 andgreater. See Table 4.

For each HC CDR3 residue having the diversity <1>, equimolar ratios arepreferably not used. Rather, the following ratios are used 0.095 [G andY] and 0.048 [A, D, E, F, H, I, K, L, M, N, P, Q, R, S, T, V, and W].Thus, there is a double dose of G and Y with the other residues being inequimolar ratios. For the other diversities, e.g., KR or SG, theresidues are present in equimolar mixtures.

In the preferred libraries of this invention the eight components arepresent in the following fractions: 1 (0.10), 2 (0.14), 3 (0.25), 4(0.13), 5 (0.13), 6 (0.11), 7 (0.04) and 8 (0.10). See Table 4.

In the more preferred embodiment of this invention, the amounts of theeight components is adjusted because the first component is not complexenough to justify including it as 10% of the library. For example, ifthe final library were to have 1×10⁹ members, then 1×10⁸ sequences wouldcome from component 1, but it has only 2.6×10⁵ CDR3 sequences so thateach one would occur in ˜385 CDR1/2 contexts. Therefore, the morepreferred amounts of the eight components are 1 (0.02), 2 (0.14), 3(0.25), 4 (0.14), 510.14), 6 (0.12), 7 (0.68), 8 (0.11). In accordancewith the more preferred embodiment component 1 occurs in ˜77 CDR1/2contexts and the other, longer CDR3s occur more often.

Table 5 shows vgDNA that embodies each of the eight HC CDR3 componentsshown in Table 4. In Table 5, the oligonucleotides (ON) Ctop25, CtprmA,C8prmB, and CBot25 allow PCR amplification of each of the variegated ONs(vgDNA): C1t08, C2t10, C3t12, C4t14, C5t15, C6t17, C7t18, and C8t19.After amplification, the dsDNA can be cleaved with AfiII and BstEII (orKpnI) and ligated to similarly cleaved vector that contains theremainder of the 3-23 domain. Preferably, this vector already containsdiversity in one, or both, of CDR1 and CDR2 as disclosed herein. Mostpreferably, it contains diversity in both the CDR1 and CDR2 regions. Itis, of course, to be understood that the various diversities can beincorporated into the vector in any order.

Preferably, the recipient vector originally contains a stuffer in placeof CDR1, CDR2 and CDR3 so that there will be no parental sequence thatwould then occur in the resulting library. Table 6 shows a version ofthe V3-23 gene segment with each CDR replaced by a short segment thatcontains both stop codons and restriction sites that will allow specificcleavage of any vector that does not have the stuffer removed. Thestuffer can either be short and contain a restriction enzyme site thatwill not occur in the finished library, allowing removal of vectors thatare not cleaved by both AfiII and BstEII (or AionI) and religated.Alternatively, the stuffer could be 200-400 bases long so that uncleanedor once-cleaved vector can be readily separated from doubly cleavedvector.

Human Antibody Light Chain: Sequence and Length Diversity

(i) Kappa Chain

(a) Framework

In the preferred embodiment of this invention, the kappa light chain isbuilt in an A27 framework with a JK1 region. These are the most common Vand J regions in the native genes. Other frameworks, such as 012, L2,and All, and other J regions, such as JK4, however, may be used withoutdeparting from the scope of this invention.

(b) CDR1

In native human kappa chains, CDR1s with lengths of 11, 12, 13, 16, and17 were observed with length 11 being predominant and length 12 beingwell represented. Thus, in the preferred embodiments of this inventionLC CDR1s of length 11 and 12 are used in an and mixture similar to thatobserved in native antibodies), length 11 being most preferred. Length11 has the following sequence: RASQ<1>V<2><2><3>LA (SEQ ID NO:14) andLength 12 hag the following sequence: RASQ<1>V<25<2><2><3>LA (SEQ IDNO:15), wherein <1> is an equimolar mixture of ill of the native-aminoacid residues, except C, <2> is 0.2 S and 0.044 of each ofADEFGHIKLMNPQRTVWY, and <3> is 0.2.Y and 0.044 each of A, D, E, F, G, H,1, K, L, M, N, Q, R, T, V, W and S. In the most preferred embodiment ofthis invention, both CDR1. lengths are used. Preferably, they arepresent in a ratio of 11:12::154:73:0.68:0.32.

(c) CDR2

In native kappa, CDR2 exhibits only length 7. This length is used in thepreferred embodiments of-this invention. It has the sequence<1>AS<2>R<4><1>, wherein <1> is an-equimolar mixture of amino acidresidues ADEFGHIKLMNPQRSTVWY; <2> is 0.2 S and 0.004 of each ofADEFGHIKLMNPQRTVWY; and <4> is 0.2 A and 0.044 of each ofDEFGHIKLMNPQRSTUWY.

(d) CDR3

In native kappa, CDR3 exhibits lengths of 4, 6, 7; 8, 9, 10, 11, 12, 13,0 and 19. While any of these lengths and mixtures of them can beemployed in this invention, we prefer lengths 8, 9 and 10, length 9being more preferred. For the preferred Length 9, the sequence is,QQ<3><1><1><1>P<1>T, wherein <1> is an equimolar mixture of amino acidresidues ADEFGHIKLMNPQRSTVWY and <3> is 0.2? and 0.044 each ofADEFGHIKLWQRSVW. Length 8 is preferably QQ33111P and Length 10 isPreferably QQ3211PP1T, wherein 1 and 3 are as defined for Length 9 and 2is S (0.2) and 0.044 each of ADEFGHIKLMNPQRTVWY. A mixture of all 3lengths being most preferred (ratios as in native antibodies), i.e.,8:9:10i28:166:63::0.1:0.65:0.25.

Table 7 shows a kappa chain gene of this invention, including a PlacZpromoter a ribosome-binding site, and signal sequence (MI3 III signal).The DNA sequence encodes the GLG amino acid sequence but does notcomprise the GLG DNA sequence. Restriction sites are designed to fallwithin each framework region so that diversity can be cloned into theCDRs. XmaI and Espl are in FR1, SexAI is in FR2, RsrII is in FR3, andKpnI (or Acc65I), are in FR4. Additional sites are provided in theconstant kappa chain to facilitate construction of the gene.

Table 7 also shows a suitable scheme of variegation for kappa. In CDR1,the most preferred length 11 is depicted. However, most preferably bothlengths 11 and 12 are used. Length 12 in CDR1 can be construed byintroducing codon 51 as <2> (i.e. a Ser-biased mixture). CDR2 of kappais always 7 codons. Table 7 shows a preferred variegation scheme forCDR2. Table 7 Shows a variegation scheme for the most preferred CDR3(length 9). Similar variegations can be lied for CDRs of length 8 and10. In the preferred embodiment of this invention, those three lengths(8, 9 and 10) are included in the libraries of this invention in thenative ratios, as described above.

Table 9 shows series of diversity oligonucleotides and primers that maybe used to construct the kappa chain diversities depicted in Table 7.

(ii) Lambda Chain

(a) Framework

The lambda chain is preferably built in a 2a2 framework with an L2Jregion. These are the most common V and J regions in the native genes.Other frameworks, such as 31, 4b, 1a and 6a, and other J regions, suchas L1J, L3J and L7J, however, may be used without departing from thescope of this invention.

(b) CDR1

In native human lambda chains, CDR1s with length 14 predominate, lengths11, 12 and 13 also occur. While any of these can be used in thisinvention, lengths 11 and 14 are preferred. For length 11 the sequenceis: TG<2><4>L<4><4><4><3><4><4> (SEQ ID NO:22) and for Length 14 thesequence is: TG<1>SS<2>VG<1><3><2><3>VS (SEQ ID NO:18), wherein <1> is0.27 T, 0.21 G and 0.027 each of ADEFHIKLMNPQRSVWY; <2> is 0.27 D, 0.27N and 0.027 each of AEFGHIKLMPQRSTVWY; <3> is 0.36 Y and 0.0355 each ofADEFGHIKLMNPQRSTVW; and <4> is an equimolar mixture of amino acidresidues ADEFGHIKLMNPQRSTVWY. Most preferably, Mixtures (similar tothose occurring in native antibodies) preferably, the ratio is11:14::23:46::0.33:0.67 of the three lengths are used.

(c) CDR2

In native human lambda chains₄.CDR2s with length 7 are by far the mostcommon. This length is preferred in this invention. The sequence of thisLength 7 CDR2 is <4><4><4><2>RPS, wherein <2> is 0.27 D, 0.27 N, and0.027 each of AEFGHIKLMPQRTVWY and <4> is an equimolar mixture of aminoacid residues ADEFGHIKLMNPQRSTVW.

(d) CDR3

In native human lambda chains, CDR3s of length 10 and 11 predominate,while length 9 is also common. Any of these three lengths can be used inthe invention. Length 11 is preferred and mixtures of 10 and 11 morepreferred. The sequence of Length 11 is <4><5><4><2><4>S<4><4><4><4>V,where <2> and <4> are as defined for the lambda CORI and <5> is 0.36 Sand 0.0355 each of ADFFGHIKLMNFORTVWY. The sequence of Length 10 is<5>SY<1><5>S<5><1><4>V (SEQ ID NO:19), wherein <1> is an equimolarmixture of ADEFGHIKLMNPQRSTVWY; and <4> and <5> are as defined forLength 11. The preferred mixtures of this invention comprise anequimolar mixture of Length 10 and Length 11. Table 8 shows a preferredfocused lambda light chain diversity in accordance with this invention.

Table 9 shows a series of diversity oligonucleotides and primers thatmay be used to construct 10 the lambda chain diversities depicted inTable 7.

Method of Construction of the Genetic Package

The diversities of heavy chain and the kappa and lambda light chains arebest constructed in separate vector's. First a synthetic gene isdesigned to embody each of the synthetic variable domains. The lightchains are bounded by restriction sites for ApaLI (positioned at thevery end of the signal sequence) and AscI (positioned after the stopcodon). The heavy chain is bounded by SfiI (positioned within the PelBsignal sequence) and NotI (positioned in the linker between CH1 and theanchor protein). Signal sequences other than PelB may also need, e.g., aM13 pIII signal sequence.

The initial genes are made with “stuffer” sequences in place of thedesired CDRs. A “stuffer” is a sequence that is to be cut away andreplaced by diverse DNA but which does not allow expression ‘of afunctional antibody gene. For example, the stuffer may contain severalstop codons and restriction sites that will not occur in the correctfinished library vector. For example, in Table 10, the stuffer for CDR1of kappa A27 contains a StuI site. The vgDNA for CDR1 is introduced as acassette from EspI, XmaI, or Af1II to dither SexAI or KasI. After theligation, the DNA is cleaved with Still; there should be no StuI sitesin the desired vectors.

The sequences of the heavy chain gene with stuffers is depicted in Table6. The sequences of the kappa light chain gene with stuffers is depictedin Table 10. The sequence of the lambda light chain gene with stuffersis depicted in Table 11.

In another embodiment of the present invention the diversities of heavychain and the kappa or lambda light chains are constructed in a singlevector or genetic packages (e.g., for display or display and expression)having appropriate restriction sites that allow cloning of these chains.The processes to construct such vectors are well known and widely usedin the art. Preferably, a heavy chain and Kappa light Chain library anda heavy chain and lambda light chain library would be preparedseparately. The two libraries, most preferably, will then be mixed inequimolar amounts to attain maximum diversity.

Most preferably, the display is had on the surface of a derivative ofM13 phage. The most preferred vector contains all the genes of M13, anantibiotic resistance-gene, and the display cassette. The preferredvector is provided with restriction sites that allow introduction andexcision of members of the diverse family of genes, as cassettes. Thepreferred vector is stable against rearrangement under the growthconditions used to amplify phage.

In another embodiment of this invention, the diversity captured by themethods of the present invention may be displayed and/or expressed in aphagemid vector (e.g., pCES1) that displays and/or expresses thepeptide, polypeptide or protein. Such vectors may also be used to storethe diversity for subsequent display and/or expression using othervectors or phage.

In another embodiment of this invention, the diversity captured by themethods of the present invention may be displayed and/or expressed in ayeast vector.

TABLE 1 3-23:JH4 CDR1/2 diversity = 1.78 × 10⁸FR1 (VP47/V3-23)--------------- 20  21 22 23 24 25 26 27 28 29 30(SEQ ID NO: 99)  A  M  A  E   V   Q   L   L   E   S   G ctgtctgaaccc atg gcc gaa/gtt/caa/ttg/tta/gag/tct/ggt/ Scab..... NcoI....      MfeI     ---------- FR1---------------------------------       31  32  33  34  35  36   37 38  39  40  41  42  43 44  45        G   G   L   V   Q   P   G   G   S   L   R   L   S  C   A     /ggc/ggt/ctt/gtt/cag/cct/ggt/ggt/tct/tta/cgt/ctt/tct/tgc/gct/        Sites of variegation        <1><1> <1> <1>   6859-fold diversity     ----FR1------------- >/ .. CDR1........... ./---FR2-----      46  47  48  49  50  51  52  53  54  55  56  57  58  59  60       A   S   G   F   T   F   S   -   Y   -   M   -   W   V   R     /gct/tcc/gga/ttc/act/ttc/tct/ - /tac/ - /atg/ - /tgg/gtt/cgc/         BspEI                       BsiWI                      BstXI.                       Sites of variegation-><2>       <2> <3>     -----FR2--------------------   >/   ..CDR2     61   62  63  64  65  66  67  68  69  70  71  72  73  74  75     Q    A   P   G   K   G   L   E   W   V   S   -   I   -   -    /caa/gct/cct/gtt/aaa/ggt/ttg/gag/tgg/gtt/tct/ - /atc/ - / - / ...BstXI              <1>     <1> 25992-fold diversity in DCR2 ...CDR2..................................... /---FR3----- 76  77  78  79  80  81  82  83  84  85  86  87  88  89  90  S   G   G   -   T   -   Y   A   D   S   V   K   G   R   F/tct/ggt/ggc/ - /act/ - /tat/gct/gac/tcc/gtt/aaa/ggt/cgc/ttc/-- - - FR3------------------------------------------------- 91  92  93  94   95  96  97  98  99 100 101 102 103 104 105 T    I   S   R   D   N   S   K   N   T   L   Y   L   Q   M/act/atc/tct/aga/gac/aac/tct/aag/aat/act/ctc/tac/ttg/cag/atg/         XbaI---FR3------------------------------------------------------ 106 107 108 109 110 111 112 113 114 115 116 117 118 119 120  N   S   L   R   A   E   D   T   A   V   Y   Y   C   A   K/aac/agc/tta/agg/gct/gag/gac/acc/gct/gtc/tac/tac/tgc/gcc/aaa/      Af1II .....CDR3................../ Replaced by the various components! 121 122 123 124 125 126 127  D   Y   E   G   T   G   Y   (SEQ ID NO: 24)/gac/tat/gaa/ggt/act/ggt/tat/ (SEQ ID NO: 23)/---------- fr4 ---(JH4)--------------------------------------------------   Y   F   D   Y     W  G   Q   G   T   L   V   T   V   S   S (SEQ ID NO: 26)/tat/ttc/gat/tat/tgg/ggt/caa/ggt/acc/ctg/gtc/acc/gtc/tct/agt/.(SEQ ID NO: 25)                              KpnI               BstEII <1> = Codons forADEFGHIKLMNPQRSTVWY (equimolar mixture) <2> = Codons for YRWVGS(equimolar mixture) <3> = Codons for PS or PS and G (equimolar mixture)

TABLE 2 Oligonucleotides used to variegate CDR1 of human HCCDR1-5 residues (ON-R1V1vg):5′-ct/tcc/gga/ttc/act/ttc/tct/<1>/tac/<1>/atg/<1>/tgg/gtt/cgc/caa/gct/cct/gg-3′(SEQ ID NO: 27) <1> = Codons of ADEFGHIKLMNPQRSTVWY 1:1 (ON-Rltop):5′-cctactgtct/tcc/gga/ttc/act/ttc/tct-3′ (SEQ ID NO: 28)(ON-Rlbot) [RC]: 5′-′tgg/gtt/cgc/caa/gct/cct/ggttgctcactc-3′(SEQ ID NO: 29) CDR1-7 residues (ON-R1V2vg):5′-ct/tcc/gga/ttc/act/ttc/tcty/<6>/<7>/<7>/tac/tac/tgg/<7>/tgg/gtt/cgc/caa/gct/cct/gg-3′ (SEQ ID NO: 30) <6> = Codons for ST, 1:1 <7>0.2025(Codons for SG) + 0.035(Codons for ADEFHIKLMNPQRTVWY)CDR1-14 residues (ON-R1V3vg):5′-ct/tcc/gga/ttc/act/ttc/tct/atc/agc/ggt/ggt/tct/atc/tcc/<1>/<1>/<1>/-tac/tac/tgg/<1>/tgg/gtt/cgc/caa/gct/cct/gg-3′ (SEQ ID NO: 31) <1> =Codons for ADEFGHIKLMNPQRSTVWY 1:1

TABLE 3 Oligonucleotides used to variegate CDR2 of human HCCDR2-17 residues (ON-R2V1vg):5′-ggt/ttg/gag/tgg/gtt/tct/<2>/atc/<2>/<3>/tct/ggt/ggc/<1>/act/<1>/tat/gct/-gac/tcc/gtt/aaa/gg-3′ (SEQ ID NO: 32) (ON-R2top):5′-ct/tgg/gtt/cgc/caa/gct/cct/ggt/aaa/ggt/ttg/gag/tgg/gtt/tct-3′(SEQ ID NO: 33) (ON-R2bot) [RC]:5′-tat/gct/gac/tcc/gtt/aaa/ggt/cgc/ttc/act/atc/tct/aga/ ttcctgtcac-3′(SEQ ID NO: 34) <I> =Codons for A, D, E, F, G, H, I, K, L, M, N, P, Q, R, S, T, V, W and Y (equimolar mixture)<2> = Codons for Y, R, W, V, G and S (equimolar mixiure) <a> =Codons for P and S (equimolar mixture) or P, S and G (equimolar mixture)(ON-R2V2vg):5′-ggt/ttg/gag/tgg/gtt/tct/<1>/atc/<4>/<1>/<1>/ggt/<5>/<1>/<1>/<1>/tat/gct/-gac/tcc/gtt/aaa/gg-3′ (SEQ ID NO: 35) <4> =Codons for DINSWY (equimolar mixture) <5> =Codons for SGDN, (equimolar mixture) CDR2-16 residues (ON-R2V3vg):5′-ggt/ttg/gag/tgg/gtt/tct/<1>/att/<4>/<1>/<1>/ggt/<5>/<1>/<1>/tat/aac/cct/tcc/ctt/aag/gg-3′ (SEQ ID NO: 36)(ON-R2bo3) [RC]:5′-tat/aac/cct/tcc/ctt/aag/ggt/cgc/ttc/act/atc/tct/aga/ttcctgtcac-3′(SEQ ID NO: 37) CDR2 19 residues (ON-R2V4vg):5′-ggt/ttg/gag/tgg/gtt/tct/<1>/atc/<8>/agt/<1>/<1>/<1>/ggt/ggt/act/act/<1>/tat/gcc/gct/tcc/gtt/aag/gg-3′ (SEQ ID NO: 38)(ON-R2bo4) [RC]:5′-tat/gcc/gct/tcc/gtt/aag/ggt/cgc/ttc/act/atc/tct/aga/ttcctgtcac′-3′(SEQ ID NO: 39) <1>, <2>, <3>, <4> and <5> are as defined above <8>is 0.27 R and 0.027 each of ADEFGHIKLMNPQSTVWY

TABLE 4 Preferred Components Fraction Preferred of Adjusted ComponentLength Complexity Library Fraction 1 YYCA21111YFDYWG. 8 2.6 × 10⁵ .10.02 (SEQ ID NO: 6) (1 = any amino acid residue, except C; 2 = K and R) 2YYCA2111111YFDYWG. 10 9.4 × 10⁷ .14 .14 (SEQ ID NO: 7) (1 =any amino acid residue, except C; 2 = K and R) 3 YYCA211111111YFDYTG. 123.4 × 10¹⁰ .25 .25 (SEQ ID NO: 8) (1 = any amino acid residue,except C; 2 = K and R) 4 YYCAR111S2S3111YFDYWG. 14 1.9 × 10⁸ .13 .14(SEQ ID NO: 9) (1 = any amino acid residue, except C; 2 = S and G 3 =Y and W) 5 YYCA2111CSG11CY1YFDYWG. 15 9.4 × 10⁷ .13 .14 (SEQ ID NO: 10)(1 = any amino acid residue except C; 2 = K and R) 6YYCA211S1TIFG11111YFDYWG. 17 1.7 × 10¹⁰ .11 .12 (SEQ ID NO: 11) (1 =any amino acid residue, except C; 2 = K and R) 7YYCAR111YY2S33YY111YFDYMG. 18 3.8 × 10⁸ .04 .08 (SEQ ID NO: 12) (1 =any amino acid residue, except C; 2 = D or G; 3 = S and G) 8YYCAR1111YC2231CY111YFDYWG. 19 2.0 × 10¹¹ .10 .11 (SEQ ID NO: 13) (1 =any amino acid residue, except C; 2 = S and G; 3 = T, D, and G)

TABLE 5 Oligonucleotides used to variegate the eight components of HC CDR3(Ctop25): 5′-gctctggtcaac/tta/agg/gct/gag/g-3′ (SEQ ID NO: 40)(CtprmA): 5′-gctctggtcaac/tta/agg/gct/gag/gac/acc/gct/gtc/tac/tac/tgc/gcc-3′                    AflLL. . .  (SEQ ID NO: 41)(CBprmB)[RC]: 5′-/tac/ttc/gat/tac/tgg/ggc/caa/ggt/acc/ctg/gtc/acc/tcgctccacc-3′              (SEQ ID NO: 42)                             BstEII...(CBot25)[RC]:  5′-/ggt/acc/ctg/gtc/acc/tcgctccacc-3′ (SEQ ID NO: 43)The 20 bases at 3′ end of CtprmA are identical to the most 5′ 20 basesof each of the vgDNA molecules. Ctop25 is identical to the most 5′25 bases of CtprmA. The 23 most 3′bases of CBprmB are the reverse complement of the most 3′23 bases of each of the vgDNA molecules.CBot25 is identical to the 25 bases at the 5′ end of CBprmB. Component 1(C1t08): 5′-cc/gct/gtc/tac/tac/tgc/gcc/<2>/<1>/<1>/<1>/<1>/tac/ttc/gat/tac/tgg/ggc/caa/gg-3′(SEQ ID NO: 44) <1> = 0.095 Y + 0.095 G +0.048 each of the residues ADEFHIKLMNPQRSTVW, no C;  <2> =K and R (equimolar mixture) component 2 (C2t10): 5′-cc/gct/gtc/tac/tac/tgc/gcc/<2>/<1>/<1>/<1>/<1>/<1>/<1>/tac/ttc/gat/tac/tgg/ggc/caa/gg-3′ (SEQ ID NO: 45) <1> = 0.095 Y + 0.095 G +0.048 each of ADEFHIKLMNPQRSTVW, no C;  <2> =K and R (equimolar mixture) Component 3 (C3t12): 5′-cc/gct/gtc/tac/tac/tgc/gcc/<2>/<1>/<1>/<1>/<1>/<1>/<1>/<1>/<1>/tac/ttc/gat/tac/-tgg/ggc/caa/gg-3′ (SEQ ID NO: 46) <1> = 0.095 Y + 0.095 G +0.048 each of ADEFHIKLMNPQRSTVW, no C;  <2> =K and R (equimolar mixture) Component 4 (C4t140): 5′-cc/gct/gtc/tac/tac/tgc/gcc/cgt/<1>/<1>l<l>/tct/<2>/tct/<3>/<1>/<1>/<1>/tac/ttc/gat/-tac/tgg/ggc/caa/gg-3′ (SEQ ID NO: 47) <1> = 0.095 Y + 0.095 G +0.048 each of ADEFHIKLMNPQRSTVW, no C;  <2> =S and G (equimolar mixture);  <3> = Y and W (equimolar mixture)Component 5 (C5t15): 5′-cc/gct/gtc/tac/tac/tgc/gcc/<2>/<1>/<1>/<1>/tgc/tct/ggt/<1>/<1>/tgc/tat/<1>/tac/-ttc/gat/tac/tgg/ggc/caa/gg-3′ (SEQ ID NO: 48) <1> = 0.095 Y + 0.095 G +0.048 each of ADEFHIKLMNPQRSTVW, no C;  <2> =K and R (equimolar mixture) Component 6 (C6t17): 5′-cc/gct/gtc/tac/tac/tgc/gcc/<2>/<1>/<1>/tct/<1>/act/atc/ttc/ggt/<1>/<1>/<1>/<1>/-<1>/tac/ttc/gat/tac/tgg/ggc/caa/gg-3′ (SEQ ID NO: 49) <1> = 0.095 Y +0.095 G + 0.048 each of ADEFHIKLMNPQRSTVW, no C;  <2> =K and R (equimolar mixture) Component 7 (C7t18): 5′-cc/gct/gtc/tac/tac/tgc/gcc/cgt/<1>/<1>/<1>/tat/tac/<2>/tct/<3>/<3>/tac/tat/-<1>/<1>/<1>/tac/ttc/gat/tac/tgg/ggc/caa/gg-3′ (SEQ ID NO: 50) <1> =0.095 Y + 0.095 G + 0.048 each of ADEFHIKLMNPQRSTVW, no C; <2> = D and G(equimolar mixture); <3> = S and G (equimolar mixture) Component 8(c8t19): 5′-cc/gct/gtc/tac/tac/tgc/gcc/cgt/<1>/<1>/<1>/<1>/tat/tgc/<2>/<2>/<3>/<1>/tgc/tat/-<1>/<1>/<1>/tac/ttc/gat/tac/tgg/ggc/caa/gg-3′(SEQ ID NO: 51) <1> =0.095 Y + 0.095 G + 0.048 each of ADEFHIKLMNPQRSTVW, no C;  <2> =S and G (equimolar mixture);  <3> = TDG (equimolar mixture);

TABLE 6  3-23:: JH4 Stuffers in place of CDRs                                         FR1(DP47/V3-23)------------------------           20 21 22                      23  24  25  26  27  28  29  30           A   M  A                      E    V   Q   L   L   E   S   Gctgtctgaac cc atg gcc                    gaa/gtt/caa/ttg/tta/gag/tct/ggt/(SEQ ID NO: 99) Scab .......NcoI....                              MfeI     ---------------------------- FR1----------------------------       31  32  33  34  35  36  37  38 39  40  41  42  43  44  45       G   G   L   V   Q   P   G   G   S   L   R   L   S   C   A     /ggc/ggt/ctt/gtt/cag/cct/ggt/ggt/tct/tta/cgt/ctt/tct/tgc/gct/     ---FR1--------------------->/...CDR1 stuffer..../---FR2------      46  47  48  49  50  51  52  53  54  55  56  57  58  59  60        A   S   G   F   T   F   S   S   Y   A   /   /   W   V   R     /gct/tcc/gga/ttc/act/ttc/tct/tcg/tac/gct/tag/taa/tgg/gtt/cgc/           BspEI                     BsiWI                       BstXI.   -------FR2-------------------------------->/...CDR2 stuffer.   61  62  63  64  65  66  67  68  69  70  71  72  73  74  75    Q   A   P   G   K   G   L   E   W   V   S   /   P   R   /  /caa/gct/cct/ggt/aaa/ggt/ttg/gag/tgg/gtt/tct/taa/cct/agg/tag/...BstXI                                       AvrII..  ....CDR2 stuffer...................................../---FR3---    91  92  93  94  95  96  97  98  99  100 101 102 103 104 105    T   I   S   R   D   N   S   K   N    T   L   Y   L   Q   M  /act/atc/tct/aga/gac/aac/tct/aag/aat/act/ctc/tac/ttg/cag/atg/            XbaI   --FR3------------..> CDR3 Stuffer ------------>/  106 107 108 109 110    N   S   L   R   A (SEQ ID NO: 53) /aac/agc/tta/agg/gct/tag taa agg cct taa (SEQ ID NO: 52)       AflII                    StuI...   /-----FR4 ---(JH4)-------------------------------------------  Y   F   D   Y   W   G   Q   G   T   L   V   T   V   S   S  (SEQ ID NO: 26)/tat/ttc/gat/tat/tgg/ggt/caa/ggt/acc/ctg/gtc/acc/gtc/tct/agt/... (SEQ ID NO: 25)                              KpnI        BstEII

TABLE 7  A27:JH1 Human Kappa light chain genegaggacc attgggcccc ctccgagact ctcgagcgcaScab ......Eco0109I           XhoI            ApaIacgcaattaa tgtgagttag ctcactcatt aggcacccca ggctttacac tttatgcttc     ..-35..          Plac                      ..-10.cggctcgtat gttgtgtgga attgtgagcg gataacaatt tcacacaggaaacagctatg accatgattacgccaagctt tggagccttt tttttggaga ttttcaac (SEQ ID NO: 54)   pflMI.......         Hind IIIM13 III signal sequence (AA seg) ------------------------------ 1   2   3   4   5   6   7   8   9   10  11  12  13  14  15 M   K   K   L   L   F   A   I   P   L   V   V   P   F   Ygtg aag aag ctc cta ttt gct atc ccg ctt gtc gtt ccg ttt tac--Signal-->FR1---------------------------------------------> 16  17  18  19  20  21  22  23  24  25  26  27  28  29  30  S   H   S   A   Q   S   V   L   T   Q   S   P   G   T   L/agc/cat/agt/gca/caa/tcc/gtc/ctt/act/caa/tct/cct/ggc/act/ctt/          ApaLI...---- FR1 -------------------------------------->/ CDR1----> 31  32  33  34  35  36  37  38  39  40  41  42  43  44  45  S   L   S   P   G   E   R   A   T   L   S   C   R   A   S (SEQ ID NO: 55)/tcg/cta/agc/ccg/ggt/gaa/cgt/gct/acc/tta/agt/tgc/cgt/gct/tcc/ (SEQ ID NO: 54; Cont′d)   EspI.....                      AflII ...             XmaI...For CDR1:  <1> ADEFGHIKLMNPQRSTVWY 1:1 <2>S(0.2) ADEFGHIKLMNPQRTVWY (0.044 each) <3>Y(0.2) ADEFGHIKLMNPQRSTVW (0.044 each)(CDR1 installed as AflII-(SexAI or KasI) cassette.) For the most preferred 11 length codon 51(XXX) is omitted; for the preferred 12 length this codon is <2>       ------ CDR1--------------------- --->/--- FR2------------->            <1>    <2>   <2> xxx <3>        46  47  48  49  50  51  52  53  54  55  56  57  58  59  60         Q   -   V   -   -   -   -   L   A   W   Y   Q   Q   K   P (SEQ ID NO: 55; Cont′d)       /cag/ - /gtt/ - / - / - / - /ctt/gct/tgg/tat/caa/cag/aaa/cct/(SEQ ID NO: 54; Cont′d)                                                             SexAI....For CDR2:  <1> ADEFGHIKLMNPQRSTVWY 1:1 <2>S(0.2) ADEFGHIKLMNPQRTVWY (0.044 each) <4>A(0.2) DEFGHIKLMNPQRSTVWY (0.044 each)CDR2 installed as (SexAI or KasI) to (BamHI or RsrII) cassette.)     ----- FR2 ------------------------->/------CDR2----------->                                         <1>         <2>     <4>      61  62  63  64  65  66  67  68  69  70  71  72  73  74  75       G   Q   A   P   R   L   L   I   Y   -   A   S   -   R   - (SEQ ID NO: 55; Cont′d)     /ggt/cag/gcg/ccg/cgt/tta/ctt/att/tat/ - /gct/tct/ - /cgc/ - (SEQ ID NO: 54; Cont′d)     SexAI....   KasI....CDR2-->/--- FR3 ------------------------------------------->   <1>  76  77  78  79  80  81  82  83  84  85  86  87  88  89  90   -   G   I   P   D   R   F   S   G   S   G   S   G   T   D / - /ggg/atc/ccg/gac/cgt/ttc/tct/ggc/tct/ggt/tca/ggt/act/gac/        BamHI                 RsrII.....--------FR3------------------------------------------------> 91  92  93  94  95  96  97  98  99  100 101 102 103 104 105  F   T   L   T   I   S   R   L   E   P   E   D   F   A   V (SEQ ID NO: 55′Cont′d)/ttt/acc/ctt/act/att/tct/aga/ttg/gaa/cct/gaa/gac/ttc/gct/gtt/ (SEQ ID NO: 54; Cont′d)                     XbaI For CDR3 (Length 9):  <1>ADEFGHIKLMNPQRSTVWY 1:1 <3> Y(0.2) ADEFGHIKLMNPQRTVW (0.044 each)For CDR3 (Length 8):  QQ33111P      1 and 3 as defined for Length 9For CDR3 (Length 10):  QQ3211PP1T      1 and 3 as defined for Length 9     2 S(0.2) and 0.044 each of ADEFGHIKLMNPQRTVWYCDR3 installed as XbaI to (Styl Or BsiWI)cassette.------------->/----CDR3-------------------------->/----FR4--->                     <3> <1> <1> <1>     <1> 106 107 108 109 110 111 112 113 114 115 116 117 118 119 120  Y   Y   C   Q   Q   -   -   -   -   P   -   T   F   G   Q (SEQ ID NO: 55; Cont′d)/tat/tat/tgc/caa/cag/ - / - / - / - /cct/ - /act/ttc/ggt/caa/ (SEQ ID NO: 54; Cont′d)              BstXI......... ----FR4-------------------->/              <-------Ckappa ------------- 121 122 123 124 125 126 127                 128 129 130 131 132 133 134  G   T   K   V   E   I   K                   R   T   V   A   A   P   S/ggt/acc/aag/gtt/gaa/atc/aag/               /cgt/acg/gtt/gcc/gct/cct/agt/      StyI....                                BsiWI.. 135 136 137 138 139 140 141 142 143 144 145 146 147 148 149  V   F   I   F   P   P   S   D   E   Q   L   K   S   G   T/gtg/ttt/atc/ttt/cct/cct/tct/gac/gaa/caa/ttg/aag/tca/ggt/act/                                      MfeI... 150 151 152 153 154 155 156 157 158 159 160 161 162 163 164  A   S   V   V   C   L   L   N   N   F   Y   P   R   E   A (SEQ ID NO: 55; Cont′d)/gct/tct/gtc/gta/tgt/ttg/ctc/aac/aat/ttc/tac/cct/cgt/gaa/gct/ (SEQ ID NO: 54; Cont′d)                                             BssSI.. 165 166 167 168 169 170 171 172 173 174 175 176 177 178 179  K   V   Q   W   K   V   D   N   A   L   Q   S   G   N   S/aaa/gtt/cag/tgg/aaa/gtc/gat/aac/gcg/ttg/cag/tcg/ggt/aac/agt/                              MluI.... 180 181 182 183 184 185 186 187 188 189 190 191 192 193 194  Q   E   S   V   T   E   Q   D   S   K   D   S   T   Y   S/caa/gaa/tcc/gtc/act/gaa/cag/gat/agt/aag/gac/tct/acc/tac/tct/ 195 196 197 198 199 200 201 202 203 204 205 206 207 208 209  L   S   S   T   L   T   L   S   K   A   D   Y   E   K   H/ttg/tcc/tct/act/ctt/act/tta/tca/aag/gct/gat/tat/gag/aag/cat/  210 211 212 213 214 215 216 217 218 219 220 221 222 223 224   K   V   Y   A   C   E   V   T   H   Q   G   L   S   S   P (SEQ ID NO: 55; Cont′d) /aag/gtc/tat/GCt/TGC/gaa/gtt/acc/cac/cag/ggt/ctg/agc/ttc/cct/ (SEQ ID NO: 54; Cont′d)                                                SacI.... 225 226 227 228 229 230 231 232 233 234  V   T   K   S   F   N   R   G   E   C (SEQ ID NO: 55; Cont′d)/gtt/acc/aaa/agt/ttc/aac/cgt/ggt/gaa/tgc/taa/tag ggcgcgcc                      DsaI....                   AscI....                                                   BssHIIacgcatctctaa gcggccgc aacaggaggag (SEQ ID NO: 54; Cont′d)             NotI....

TABLE 8  2a2:JH2 Human lambda-chain gene gaggaccatt gggcccc ttactccgtgacScab...... Eco0109I         ---------FR1-------------------------------------------->         1   2   3   4   5   6   7   8   9  10  11  12  13  14  15 S   A   Q   S   A   L   T   Q   P   A   S   V   S   G   S   P   G (SEQ ID NO: 57)agt/gca/caa/tcc/gct/ctc/act/cag/cct/gct/agc/gtt/tcc/ggg/tca/cct/ggt/ (SEQ ID NO: 56) ApaLI...                            NheI...         BstEII...                                                         SexAI....For CDR1 (length 14):  <1> =0.27 T, 0.27 G, 0.027 each of ADEFHIKLMNPQRSVWY, no C <2> =0.27 D, 0.27 N,.0.027 each of AEFGHIKLMPQRSTVWY, no C <3> =0.36 Y, 0.0355 each of ADEFGHIKLMNPQRSTVW, no C                              T  G   <1>  S   S  <2>  V   G -----FR1 ---------------->   /---CDR1----------------------- 16  17  18  19  20  21  22  23  24  25  26  27  28  29  30  Q   S   I   T   I   S   C   T   G   -   S   S   -   V   G/caa/agt/atc/act/att/tct/tgt/aca/ggt/ - /tct/tct/ - /gtt/ggc/                         BsrGI..  <1> <3> <2> <3>  V   S =vg Scheme #1, length = 14 -----CDR1 ------------->/------------- FR2----------------- 31  32  33  34  35  36  37  38  39  40  41  42  43  44  45  -   -   -   -   V   S   W   Y   Q   Q   H   P   G   K   A (SEQ ID NO: 57; Cont′d)/ - / - / - / - /gtt/tct/tgg/tat/caa/caa/cac/ccg/ggc/aag/gcg/ (SEQ ID NO: 56; Cont′d)                                          XmaI....     KasI.....                                          AvaI....A second Vg scheme for CDR1 gives segments of length 11: T₂₂G<2><4>L<4><4><4><3><4><4> where <4> =equimolar mixture of each of ADEFGHIKLMNPQRSTVWY, no C <3> =as defined above for the alternative CDR1 For CDR2: <2> and <4>8 are the same variegation as for CDR1                          <4> <4><4> <2> R   P   S     --FR2--------------->/-------CDR2--------- ----->/------FR3-    46  47  48  49  50  51  52  53  54  55  56  57  58  59  60     P   K   L   M   I   Y   -   -   -   -   R   P   S   G   V   /ccg/aag/ttg/atg/atc/tac/ - / - / - / - /cgt/cct/tct/ggt/gtt/KasI.... --------FR3------------------------------------------------- 61  62  63  64  65  66  67  68  69  70  71  72  73  74  75  S   N   R   F   S   G   S   K   S   G   N   T   A   S   L (SEQ ID NO: 57; Cont′d)/agc/aat/cgt/ttc/tcc/gga/tct/aaa/tcc/ggt/aat/acc/gca/agc/tta/ (SEQ ID NO: 56; Cont′d)                  BspEI..                              HindIII.                      BsaBI..............(blunt)-------FR3-------------------------------------------------> 76  77  78  79  80  81  82  83  84  85  86  87  88  89  90  T   I   S   G   L   Q   A   E   D   E   A   D   Y   Y   C (SEQ ID NO: 57; Cont′d)/act/atc/tct/ggt/ctg/cag/gct/gaa/gac/gag/gct/gac/tac/tat/tgt/ (SEQ ID NO: 56; Cont′d)                  PstI... CDR3 (Length 11):  <2> and <4>are the same variegation as for CDR1 <5> =0.36 S, 0.0355 each of ADEFGHIKLMNPQRTVWY no C CDR3 (Length 10): <5>SY <1> <5> S <5> <1> <4> V <1>is an equimolar mixture of ADEFGHIKLMNPQRSTVWY, no C <4> and <5>are as defined for Length 11 <4> <5> <4> <2> <4> S <4> <4> <4> <4> V   ------CDR3--------------------------------->/----FR4-------    91  92  93  94  95  96  97  98  99  100 101 102 103 104 105     -   -   -   -   -   S   -   -   -   -   V   F   G   G   G   / - / - / - / - / - /tct/ - / - / - / - /gtc/ttc/ggc/ggt/ggt/                                                           KpnI..    -------FR4------------->    106 107 108 109 110 111 112 113 114 115 116 117 118 119 120     T   K   L   T   V   L   G   Q   P   K   A   A   P   S   V   /acc/aaa/ctt/act/gtc/ctc/ggt/caa/cct/aag/gct/gct/cct/tcc/gtt/KpnI...                      HincII..                                   Bsu36I...    121 122 123 124 125 126 127 128 129 130 131 132 133 134 135     T   L   F   P   P   S   S   E   E   L   Q   A   N   K   A (SEQ ID NO: 57; Cont′d)   /act/ctc/ttc/cct/cct/agt/tct/gaa/gag/ctt/caa/gct/aac/aag/gct/ (SEQ ID NO: 56; Cont′d)                                SapI.....     136 137 138 139 140 141 142 143 144 145 146 147 148 149 150      T   L   V   C   L   I   S   D   F   Y   P   G   A   V   T    /act/ctt/gtt/tgc/ttg/atc/agt/gac/ttt/tat/cct/ggt/gct/gtt/act/                      BclI....     151 152 153 154 155 156 157 158 159 160 161 162 163 164 165      V   A   W   K   A   D   S   S   P   V   K   A   G   V   E    /gtc/gct/tgg/aaa/gcc/gat/tct/tct/cct/gtt/aaa/gct/ggt/gtt/gag/                                                                 BsmBI...    166 167 168 169 170 171 172 173 174 175 176 177 178 179 180      T   T   T   P   S   K   Q   S   N   N   K   Y   A   A   S    /acg/acc/act/cct/tct/aaa/caa/tct/aac/aat/aag/tac/gct/gcg/agc/BsmBI...                                               SacI....     181 182 183 184 185 186 187 188 189 190 191 192 193 194 195      S   Y   L   S   L   T   P   E   Q   W   K   S   H   K   S (SEQ ID NO: 57; Cont′d)    /tct/tat/ctt/tct/ctc/acc/cct/gaa/caa/tgg/aag/tct/cat/aaa/tcc/ (SEQ ID NO: 56; Cont′d)SacI...  196 197 198 199 200 201 202 203 204 205 206 207 208 209 210  Y   S   C   Q   V   T   H   E   G   S   T   V   E   K   T/tat/tcc/tgt/caa/gtt/act/cat/gaa/ggt/tct/acc/gtt/gaa/aag/act/                      BspHI... 211 212 213 214 215 216 217 218 219  V   A   P   T   E   C   S (SEQ ID NO: 57; Cont′d)/gtt/gcc/cct/act/gag/tgt/tct/tag/tga/ggcgcgcc                                    AscI....                                      BssHIIaacgatgttc aag gcggccgc aacaggaggag (SEQ ID NO: 56; Cont′d)               NotI.... Scab.......

TABLE 9  Oligonucleotides For Kappa and Lambda Light Chain Variegation(Ctop25): 5′-gctctggtcaac/tta/agg/gct/gag/g-3′ (SEQ ID NO: 58)(CtprmA): 5′-gctctggtcaac/tta/agg/gct/gag/gac/acc/gct/gtc/tac/tac/tgc/gcc-3′           (SEQ ID NO: 59) AflII...(CBprmB)[RC]: 5′-/tac/ttc/gat/tac/ttg/ggc/caa/ggt/acc/ctg/gtc/acc/tcgctccacc-3′             (SEQ ID NO: 60)                            BstEII...(CBot25) [RC]: 5′-/ggt/acc/ctg/gtc/acc/tcgaccacc-3′ (SEQ ID NO: 61)Kappa chains: CDR1 (“1”), CDR2 (“2”), CDR1 (“3”) CDR1(KalTop610): 5′-ggtctcagttg/cta/agc/ccg/ggt/gaa/cgt/gct/acc/tta/agt/tgc/cgt/gct/tcc/cag-3′                (SEQ ID NO: 62)(KalSTp615): 5′-ggtctcagttg/cta/agc/ccg/ggt/g-3′ (SEQ ID NO: 63)(KalBot620) [RC]: ′5′-ctt/gct/tgg/tat/caa/cag/aaa/cct/ggt/cag/gcg/ccaagtcgtgtc-3′                   (SEQ ID NO: 64)(KalSB625) [RC]: 5′-cct/ggt/cag/gcg/ccaagtcgtgtc-3′ (SEQ ID NO: 65)(Kalvg600): 5′-gct/acc/tta/agt/tgc/cgt/gct/tcc/cag-      /<1>/gtt/<2>/<2>/<3>/ctt/gct/tgg/tat/caa/cag/aaa/cc-3′(SEQ ID NO: 66) (Kalvg600-12): 5′-gct/acc/tta/agt/tgc/cgt/gct/tcc/cag-      /<1>/gtt/<2>/<2>/<2>/<3>/ctt/gct/tgg/tat/caa/cag/aaa/cc-3′(SEQ ID NO: 67) CDR2 (Ka2Tshort657): 5′-cacgagtccta/cct/ggt/cag/gc-3′(SEQ ID NO: 68)(Ka2Tlong655): 5′-cacgagtccta/cct/ggt/cag/gcg/ccg/cgt/tta/ctt/att/tat-3′(SEQ ID NO: 69) (Ka2Bshort660): [RC]: 5′-/gac/cgt/ttc/tct/ggt/tctcacc-3′(SEQ ID NO: 70)(Ka2vg650): 5′-cag/gcg/ccg/cgt/tta/ctt/att/tat/<1>/gct/tct/<2>/-                  /cgc/<4>/<1>/ggg/atc/ccg/gac/cgt/ttc/tct/ggt/tctcacc-3′(SEQ ID NO: 71) CDR3(Ka3Tlon672): 5′-gacgagtocttct/aga/ttg/gaa/cct/gaa/gac/ttc/gct/gtt/tat/tat/tgc/caa/c-3′              (SEQ ID NO: 72)(Ka3BotL682)[RC]: 5′-act/ttc/ggt/caa/ggt/acc/aag/gtt/gaa/atc/aag/cgt/acg/tcacaggtgag-3′                 (SEQ ID NO: 73)(Ka3Bsho694) [RC]: 5′-gaa/atc/aag/cgt/acg/tcacaggtgag-3′(SEQ ID NO: 74)(Ka3vg670): 5′-gac/ttc/gct/gtt/ -              /tat/tat/tgc/caa/cag/<3>/<1>/<1>/<1>/cct/<1>/act/ttc/ggt/caa/-              /ggt/acc/aag/gtt/g-3′ (SEQ ID NO: 75)(Ka3v670-8): 5′-gac/ttc/gct/gtt/-            /tat/tat/tgc/caa/cag/<3>/<3>/<1>/<1>/<1>/cct/ttc/ggt/caa/-            /ggt/acc/aag/gtt/g-3′ (SEQ ID NO: 76)(Ka3vg670-10): 5′-gac/ttc/gct/gtt/tat/-             /tat/tgc/caa/cag/<3>/<2>/<1>/<1>/cct/cct/<1>/act/ttc/ggt/caa/-             /ggt/acc/aag/gtt/g-3′ (SEQ ID NO: 77)Lambda Chains:  CDR1 (“1”), CDR2 (“2”), CDR3(“3”) CDR1(LmlTPri75): 5′-gacgagtcctgg/tca/cct/ggt/-3′ (SEQ ID NO: 78)(Lm1t1o715): 5′-gacgagtcctgg/tca/cct/ggt/caa/agt/atc/act/att/tct/tgt/aca/ggt-3′             (SEQ ID NO: 79)(Lm1b1o724)[rc]: 5′-/gtt/tct/tgg/tat/caa/caa/cac/ccg/ggc/aag/gcg/agatcttcacaggtgag-3′                 (SEQ ID NO: 80)(Lm1bsh737)[rc]: 5′-gc/aag/gcg/agatcttcacaggtgag-3′ (SEQ ID NO: 81)(Lm1vg710b): 5′-gt/atc/act/att/tct/tgt/aca/ggt/<2>/<4>/ctc/<4>/<4>/<4>/-                    /<3>/<4>/<4>/tgg/tat/caa/caa/cac/cc-3′(SEQ ID NO: 82)(Lmlvg710): 5′-gt/atc/act/att/tct/tgt/aca/ggt/<1>/tct/tct/<2>/gtt/ggc/-       /<1>/<3>/<2>/<3>/gtt/tct/tgg/tat/caa/caa/cac/cc-3′(SEQ ID NO: 83) CDR2(Lm2TSh757): 5′-gagcagaggac/ccg/ggc/aag/gc-3′(SEQ ID NO: 84)(Lm2TLo753): 5′-gagcagaggac/ccg/ggc/aag/gcg/ccg/aag/ttg/atg/atc/tac/-3′(SEQ ID NO: 85)(Lm2BLo762) [RC]: 5′-cgt/cct/tct/ggt/gtc/agc/aat/cgt/ttc/tcc/gga/tcacaggtgag-3′                 (SEQ ID NO: 86)(Lm2Bsh765) [RC]: 5′-cgt/ttc/tcc/gga/tcacaggtgag-3′ (SEQ ID NO: 87)(Lm2vg750): 5′-g/ccg/aag/ttg/atg/atc/tac/-    <4>/<4>/<4>/<2>/cgt/cct/tct/ggt/gtc/agc/aat/c-3′ (SEQ ID NO: 88)CDR3 (Lm3TSh822): 5′-ctg/cag/gct/gaa/gac/gag/gct/gac-3′ (SEQ ID NO: 89)(Lm3TLo819): 5′-ctg/cag/gct/gaa/gac/gag/gct/gac/tac/tat/tgt/-3′(SEQ ID NO: 90)(Lm3BLo825) [RC]: 5′-gtc/ttc/ggc/ggt/ggt/acc/aaa/ctt/act/gtc/ctc/ggt/caa/cct/aag/g-                  acacaggtgag-3′ (SEQ ID NO: 91) (Lm3BSh832) (RC]: 5′c/ggt/caa/cct/aag/gacacaggtgag (SEQ ID NO: 92)(Lm3vg17): 5′-gac/gag/gct/gac/tac/tat/tgt/-/     <4>/<5>/<4>/<2>/<4>/tct/<4>/<4>/<4>/<4>/-                  Gtc/ttc/ggc/ggt/ggt/acc/aaa/ctt/ac-3′ (SEQ ID NO: 93)(Lm3vg817-10): 5′- gac/gag/gct/gac/tac/tat/tgt/-       /<5>/agc/tat/<1>/<5>/tct/<5>/<1>/<4>/gtc/ttc/ggc/ggt/ggt/-       /acc/aaa/ctt/ac-3′ (SEQ ID NO: 94)

TABLE 10  A27:JH1 Kappa light chain gene with stuffers in place of CDRsEach stuffer contains at least one stop codon and arestriction site that will be unique within the diversity vector.gaggacc attgggcccc ctccgagact ctcgagcgca    Scab..... EcoO109I             ApaI.             XhoI..acgcaattaa tgtgagttag ctcactcatt aggcacccca ggctttacac tttatgcttc      ..−35..         Plac                     ..−10.cggctcgtat gttgtgtgga attgtgagcg gataacaatt tcacacagga aacagctatgaccatgatta cgccaagctt tggagccttt tttttggaga ttttcaac (SEQ ID NO:95)           Pf1MI .............               Hind3.M13 III signal sequence (AA seq)--------------------------> 1   2   3   4   5   6   7   8   9  10  11  12  13  14  15 M   K   K   L   L   F   A   I   P   L   V   V   P   F   Ygtg aag aag ctc cta ttt gct atc ccg ctt gtc gtt ccg ttt tac --Signal-->FR1-------------------------------------------- 16  17  18  19  20  21  22  23  24  25  26  27  28  29  30  S   H   S   A   Q   S   V   L   T   Q   S   P   G   T   L/agc/cat/agt/gca/caa/tcc/gtc/ctt/act/caa/tct/cct/ggc/act/ctt/         ApaLI...----- FR1------------------- -------------->/---------Stuffer-> 31  32  33  34  35  36  37  38  39  40  41  42  43  S   L   S   P   G   E   R   A   T   L   S   /   / (SEQ ID NO: 96)/tcg/cta/agc/ccg/ggt/gga/cgt/gct/acc/tta/agt/tag/taa/gct/ccc/ (SEQ ID NO: 95; Cont′d)   EspI.....                      AflII...            XmaI....- Stuffer for CDR1--> FR2 --------------- FR2--- >/ Stuffer for CDR2                       59  60  61  62  63  64  65 66                        K   P   G   Q   A   P   R/agg/cct/ctt/tga/tct/g/aaa/cct/ggt/cag/gcg/ccg/cgt/taa/tga/aagcgctaatggccaacagtgStuI...                 SexAI...    KasI....               AfeI..   MscI..Stuffer-->/--- FR3 -------------------------------------------> 76  77  78  79  80  81  82  83  84  85  86  87  88  89  90  T   G   I   P   D   R   F   S   G   S   G   S   G   T   D (SEQ ID NO: 96; Cont′d)/act/ggg/atc/ccg/gac/cgt/ttc/tct/ggc/tct/ggt/tca/ggt/act/gac/ (SEQ ID NO: 95; Cont′d)       BamHI...              RsrII............--------FR3------>----------------STUFFER for CDR3-------------------> 91  92  93  94  95  96  97   F   T   L   T   I   S   R   /   //ttt/acc/ctt/act/att/tct/aga/taa/tga/ gttaac tag acc tacgta acc tag                     XbaI...          HpaI..         SnaBI.----------------------CDR3 stuffer---------------->/------FR4------->                                                         118 119 120                                                           F   G   Q                                                        /ttc/ggt/caa/-----FR4-------------------->            <--------Ckappa ----------- 121 122 123 124 125 126 127              128 129 130 131 132 133 134  G   T   K   V   E   I   K                R   T   V   A   A   P   S (SEQ ID NO: 96; Cont′d)/ggt/acc/aag/gtt/gaa/atc/aag/            /cgt/acg/gtt/gcc/gct/cct/agt/      StyI....                            BsiWI..             (SEQ ID NO: 95; Cont′d) 135 136 137 138 139 140 141 142 143 144 145 146 147 148 149  V   F   I   F   P   P   S   D   E   Q   L   K   S   G   T (SEQ ID NO: 96; Contfd)/gtg/ttt/atc/ttt/cct/cct/tct/gac/gaa/caa/ttg/aag/tca/ggt/act/                                      MfeI...acgcatctctaa gcggccgc aacaggaggag (SEQ ID NO: 95; Cont′d)             NotI....                EagI..

TABLE 11  2a2:JH2 Human lambda-chain gene with stuffers in place of CDR3gaggaccatt gggcccc ttactccgtgac Scab.....  EcoO109I            ApaI         ----------FR1-------------- ------------------------------>         1   2   3   4   5   6   7   8   9  10  11  12  13  14  15 S   A   Q   S   A   L   T   Q   P   A   S   V   S   G   S   P   Gagt/gca/caa/tcc/gct/ctc/act/cag/cct/gct/agc/gtt/tcc/ggg/tca/cct/ggt/ApaLI...                            NheI...         BstEll...                                                          SexAI....-------FR1----------------> /---------stuffer for CDR1 --------- 16  17  18  19  20  21  22  23  Q   S   I   T   I   S   C   T (SEQ ID NO: 98)/caa/agt/atc/act/att/tct/tgt/aca/tct tag tga ctc (SEQ ID NO: 97)                         BsrGI..----Stuffer----------------------------->--------FR2------->31  32  33  34  35  36  37  38  39  40  41  42  43  44  45 R   S   /    /  P   /                   H   P   G   K   Aaga tct taa tga ccg tag                 cac/ccg/ggc/aag/gcg/ BglII                                    XmaI....     KasI.....                                          AvaI.... --/-------------Stuffer for CDR2--------------------------------->   P /ccg/taa/tga/atc tcg tac g                          ct/ggt/gtt/KasI....          BsiWI...-------FR3------------------------------------------------ 61   62 63  64  65  66  67  68  69  70  71  72  73  74  75  S   N   R   F   S   G   S   K   S   G   N   T   A   S   L (SEQ ID NO: 98; Cont′d)/agc/aat/cgt/ttc/tcc/gga/tct/aaa/tcc/ggt/aat/acc/gca/agc/tta/ (SEQ ID NO: 97; Cont′d)             BseEI..                               HindIII.                    BsaBI..........(blunt)------FR3------------->/--Stuffer for ODR3------------------>/         76  77  78  79  80  81  82  83  84  85  86 87  88  89  90  T   I   S   G   L   Q/act/atc/tct/ggt/ctg/cag/gtt ctg tag ttc caattg ctt tag tga ccc                 PstI...                 MfeI..-----Stuffer------------------------------->/---FR4---------                                               103 104 105                                                G   G   G                                              /ggc/ggt/ggt/                                                        KpnI...--------FR4--------------> 106 107 108 109 110 111 112 113 114 115 116 117 118 119 120   T   K   L   T   V   L   G   Q   P   K   A   A   P   S (SEQ ID NO: 98; Cont′d)V/acc/aaa/ctt/act/gtc/ctc/ggt/caa/cct/aag/gct/gct/cct/tcc/gtt/ (SEQ ID NO: 97; Cont′d)KpnI...                      HincII..                                  Bsu36I...121 122 123 124 125 126 127 128 129 130 131 132 133 134 135  T   L   F   P   P   S   S   E   E   L   Q   A   N   K   A/act/ctc/ttc/cat/cct/agt/tct/gaa/gag/ctt/caa/gct/aac/aag/gct/                             SapI..... 136 137 138 139 140 141 142 143 144 145 146 147 148 149 150  T   L   V   C   L   I   S   D   F   Y   P   G   A   V   T (SEQ ID NO: 98; Cont′d)/act/cct/gtt/tgc/ttg/atc/agt/gac/ttt/tat/cct/ggt/gct/gtt/act/ (SEQ ID NO: 97; Cont′d)                  Bc1I....

The invention relates to generation of useful diversity in syntheticantibody (Ab) gene, especially to Ab genes having frameworks derivedfrom human Abs.

BACKGROUND OF THE INVENTION

Antibodies are highly useful molecules because of their ability to bindalmost any substance with high specificity and affinity and theirability to remain in circulation in blood for prolonged periods astherapeutic or diagnostic agents. For treatment of humans, Abs derivedfrom human Abs are much preferred to avoid immune response to the Ab.For example, murine Abs very often cause Human Anti Mouse Antibodies(HAMA) which at a minimum prevent the therapeutic effects of the murineAb. For many medical applications, monoclonal Abs are preferred.Nowadays the preferred method of obtaining a human Ab having aparticular binding specificity is to select the Ab from a library ofhuman-derived Abs displayed on a genetic package, such as filamentousphage.

Libraries of phage-displayed Fabs and scFvs have been produced inseveral ways. One method is to capture the diversity of donors, eithernaive or immunized. Another way is to generate libraries havingsynthetic diversity. The present invention relates to methods ofgenerating useful diversity in human Ab scaffolds.

As is well known, typical Abs consist of two heavy chains (HC) and twolight chains (LC). There are several types of HCs: gamma, mu, epsilon,delta, etc. Each type has an N-terminal V domain followed by three ormore constant domains. The LCs comprise an N-terminal V domain followedby a constant domain. LCs come in two types: kappa and lambda.

Within each V domain (LC or HC) there are seven canonical regions, namedFR1, CDR1, FR2, CDR2, FR3, CDR3, and FR4, where “FR” stands for“Framework Region” and “CDR” stands for “Complementarity DeterminingRegion”. For LC and HC, the FR and CDR GLGs have been selected over timeto be secretable, stable, non-antigenic and these properties should bepreserved as much as possible. Actual Ab genes contain mutations in theFR regions and some of these mutations contribute to binding, but suchuseful FR mutations are rare and are not necessary to obtainhigh-affinity binding. Thus, the present invention will concentratediversity in the CDR regions.

In LC, FR1 up to FR3 and part of CDR3 comes from a genomic collection ofgenes called “V-genes”. The remainder of CDR3 and FR4 comes from agenomic collection of genes called “J-genes”. The joining may involve acertain degree of mutation, allowing diversity in CDR3 that is notpresent in the genomic sequences. After the LC gene is formed, somaticmutations can give rise to mature, rearranged LC genes that have higheraffinity for an antigen (Ag) than does any LC encoded by genomicsequences. A large fraction of somatic mutations occur in CDRs.

The HC V region is more complicated. A V gene is joined to a J gene withthe possible inclusion of a D segment. About half of HC Abs sequencescontain a recognizable D segment in CDR3. The joining is achieved withan amazing degree of molecular sloppiness. Roughly, the end of the Vgene may have zero to several bases deleted or changed, the D segmentmay have zero to many bases removed or changed at either end, a numberof random bases may be inserted between V and D or between D and J, andthe 5′ end of J may be edited to remove or change several bases. Withal,it is amazing that human heavy chains work, but they do. The upshot isthat the CDR3 is highly diverse both in encoded amino-acid sequences andin length. In designing synthetic libraries, there is the temptation tojust throw in a high degree of synthetic diversity and let the phagesort it out. Nevertheless, D regions serve a function. They cause the Abrepertoire to be rich in sequences that a) allow Abs to fold correctly,and b) are conducive to binding to biological molecules, i.e. antigens.

One purpose of the present invention is to show how a manageablecollection of diversified sequences can confer these advantages onsynthetic Ab libraries. Another purpose of the present invention is todisclose analysis of known mature Ab sequences that lead to improveddesigns for diversity in the CDR1 and CDR2 of HC and the three CDRs oflambda and kappa chains.

BRIEF STATEMENT OF THE INVENTION

The invention is directed to methods of preparing synthetically diversepopulations of Ab genes suitable for display on genetic packages (suchas phage or phagemids) or for other regimens that allow selection ofspecific binding. Said populations concentrate the diversity intoregions of the Ab that are likely to be involved in determining affinityand specificity of the Ab for particular targets. In particular, acollection of actual Ab genes has been analyzed and the sites of actualdiversity have been identified. In addition, structural considerationswere used to determine whether the diversity is likely to greatlyinfluence the binding activity of the Ab. Schemes of variegation arepresented that encode populations in which the majority of members willfold correctly and in which there is likely to be a plurality of membersthat will bind to any given Ag. Specifically, a plan of variegation ispresented for each CDR of the human heavy chain, kappa light chain, andlambda light chain. The variegated CDRs are presented in synthetic HCand LC frameworks.

In one embodiment, the invention involves variegation of human HCvariable domains based on a synthetic 3-23 domain joined to a JH4segment in which the variability in CDR1 and CDR2 comprises sequencevariation of segments of fixed length while in CDR3 there are severalcomponents such that the population has lengths roughly corresponding tolengths seen in human Abs and having embedded D segments in a portion ofthe longer segments. In the light chains, the kappa chain is built in anA27 framework and a JK1 while lambda is built in a 2a2 framework with anL2 J region.

Examples Choice of a Heavy-Chain V Domain

The HC Germ-Line Gene (GLG) 3-23 (also known as VP-47) accounts forabout 12% of all human Abs and it suitable for the framework of thelibrary. Certain types of Ags elicit Abs having particular types of VHgenes; in some cases, the types elicited are otherwise rarely found.This apparent Ag/Ab type specificity has been ascribed to possiblestructural differences between the various families of V genes. It isalso possible that the selection has to do with the availability ofparticular AA types in the GLG CDRs. Suppose, for example, that thesequence YR at positions 4 and 5 of CDR2 is particularly effective inbinding a particular type of Ag. Only the V gene 6-1 provides thiscombination. Most Abs specific for the Ag will come from GLG 6-1. IfY4-R5 were provided in other frameworks, then other frameworks arelikely to be as effective in binding the Ag.

Analysis of HC CDR1 and CDR2:

In CDR1 and CDR2 of HCs, the GLGs provide limited length diversity asshown in Table 15P. Note that GLGs provide CDR1s only of the lengths 5,6, and 7. Mutations during the maturation of the V-domain gene leads toCDR1s having lengths as short as 2 and as long as 16. Nevertheless,length 5 predominates. The preferred length for the present invention is5 AAs in CDR1 with a possible supplemental components having lengths of7 and 14.

GLGs provide CDR2s only of the lengths 15-19, but mutations duringmaturation result in CDR2s of length from 16 to 28 AAs. The lengths 16and 17 predominate in mature Ab genes and length 17 is the mostpreferred length for the present invention. Possible supplementarycomponents of length 16 and 19 may also be incorporated.

Table 20P shows the AA sequences of human GLG CDR1s and CDR2. Table 21Pshows the frequency of each amino-acid type at each position in theGLGs. The GLGs as shown in Table 20P have been aligned by inserting gapsnear the middle of the segment so that the ends align.

The 1398 mature V-domain genes used in studying D segments (vide infra)were scanned for examples in which CDR1 and CDR2 could be readilyidentified. Of this sample 1095 had identifiable CDR1, 2, and 3. TheCDRs were identified by finding subsequences of the GLGs in an openreading frame. There are 51 human HC V genes. At the end of FR1, thereare 20 different 9-mers. At the start of FR2, there are 11 different9-mers. At the end of FR2 there are 14 different 9-mers. At the start ofFR3, there are 14 different 9-mers. At the end of FR3, there are 13different 9-mers. At the start of JH, there are three different 9-mers.These motifs were compared to the reported gene in frame and a match, atthe site of maximum similarity, of seven out of nine was deemedacceptable. Only when all three CDRs were identified were any of theCDRs included in the analysis. In addition, the type of the gene wasdetermined by comparing the framework regions to the GLG frameworks; theresults are shown in Table 22P.

Design of HC CDR1 and CDR2 Diversity.

Diversity in CDR1 and CDR2 was designed from: a) the diversity of theGLGs, b) observed diversity in mature HC genes, and c) structuralconsiderations. In CDR1, examination of a 3D model of a humanized Abshowed that the side groups of residues 1, 3, and 5 were directed towardthe combining pocket. Consequently, we allow each of these positions tobe any amino-acid type except cysteine. Cysteine can form disulfidebonds. Disulfide bonds are an important component of the canonical Igfold. Having free thiol groups could interfere with proper folding ofthe HC and could lead to problems in production or manipulation ofselected Abs. Thus, I exclude cysteine from the menu. The side groups ofresidue 2 is directed away from the combining pocket. Although thisposition shows substantial diversity, both in GLG and mature genes, Ifixed this residue as Tyr because it occurs in 681/820 mature genes(Table 21P). Position 4 is fixed as Met. There is some diversity here,but almost all mature genes have uncharged hydrophobic AA types: M, W,I, V, etc. (Table 21P). Inspection of a 3D model shows that the sidegroup of residue 4 is packed into the innards of the HC. Since we areusing a single framework (3-23), we retain the Met that 3-23 has becauseit is likely to fit very well into the framework of 3-23. Thus, the mostpreferred CDR1 library consists of XYXMX (SEQ ID NO:109) where X can beany one of [A,D,E,F,G,H,I,K,L,M,N,P,Q,R,S,T,V,W,Y] (no C). The DNA thatencodes this is preferably synthesized using trinucleotide buildingblocks so that each AA type is present in essentially equimolar amounts.Specifically, the X codons are synthesized using a mixture of the codons[gct, gat, gag, ttt, ggt, cat, att, aag, atg, aat, cct, cag, cgt, tct,act, gtt, tgg, tat]. This diversity is shown in the context of asynthetic 3-23 gene in Table 18P. The diversity oligonucleotide (ON) issynthesized from BspEI to BstXI and can be incorporated either by PCRsynthesis using overlapping ONs or introduced by ligation ofBspEI/BstXI-cut fragments. Table 22P shows ONs that embody the specifiedvariegation. PCR using ON-R1V1vg, ON-R1top, and ON-R1bot gives a dsDNAproduct of 73 base pairs, cleavage with BspEI and BstXI trims 11 and 13bases from the ends and provides cohesive ends that can be ligated tosimilarly cut vector having the synthetic 3-23 domain shown in Table18P. Replacement of ON-R1V1vg with either ONR1V2vg or ONR1V3vg allowssynthesis of the two alternative diversity patterns given below.

Alternatively, one can include CDR1s of length 7 and/or 14. For length7, a preferred diversity is (S/T)₁(S/G/x)₂(S/G/x)₃Y₄Y₅W₆(S/G/x)₇ (SEQ IDNO:107); where (S/T) indicates an equimolar mixture of Ser and Thrcodons; (S/G/x) indicates a mixture of 0.2025 S, 0.2025 G, and 0.035 foreach of A, D, E, F, H, I, K, L, M, N, P, Q, R, T, V, W, Y. Otherproportions could be used. The design gives a predominance of Ser andGly at positions 2, 3, and 7, as occurs in mature HC genes. For length14, a preferred pattern of diversity is VSGGSISXXXYYWX (SEQ ID NO:1)where X can be any AA type except Cys. This pattern appears to arise byinsertions into the GLG sequences (SGGYYWS; SEQ ID NO:110, (4-30.1 and4-31) and similar sequences. There is a preference for a hydrophobicresidue at position 1 (V or C) with a second insertion of SISXXX (SEQ IDNO:111) between GG and YY. Diversity ONs having CDR1s of length 7 or 14are synthesized from BspEI to BstXI and introduced into the library inappropriate proportions to the CDR1 of length 5. The components shouldbe incorporated in approximately the ratios in which they are observedin antibodies selected without reference to the length of the CDRs. Forexample, the sample of 1095 HC genes examined here have them in theratios (L=5:L=7:L=14::820:175:23::0.80:0.17:0.02).

CDR2

Diversity at CDR2 was designed with the same considerations: GLGsequences, mature sequences and 3D structure. A preferred length forCDR2 is 17, as shown in Table 18P. Examination of a 3D model suggeststhat the residues shown as varied in Table 18P are the most likely tointeract directly with Ag. Thus a preferred pattern of variegation is:<2>I<2><3>SGG<1>T<1>YADSVKG (SEQ ID NO:2), where <2> indicates a mixtureof YRWVGS, <3> is a mixture of P and S, and <1> is a mixture ofADEFGHIKLMNPQRSTVWY (no C). ON-R2V1vg shown in Table 22P embodies thisdiversity pattern. PCR with ON-R2V1vg, ON-R2top, and ONR2bot gives adsDNA product of 122 base pairs. Cleavage with BstXI and XbaI removesabout 10 bases from each end and produces cohesive ends that can beligated to similarly cut vector that contains the 3-23 gene shown inTable 18P.

An alternative pattern would include the variability seen in matureCDR2s as shown in Table 21P: <1>I<4><1><1>G<5><1><1><1>YADSVKG (SEQ IDNO:3), where <4> indicates a mixture of DINSWY, and <5> indicates amixture of SGDN. This diversity pattern is embodied in ON-R2V2vg shownin Table 22P. For either case, the variegated ONs would be synthesizedso that fragments of dsDNA containing the BstXI and XbaI site can begenerated by PCR. ON-R2V2vg embodies this diversity pattern.

Alternatively, one can allow shorter or longer CDR2s. Table 22P showsON-R2V3vg which embodies a CDR2 of length 16 and ON-R2V4vg whichembodies a CDR2 of length 19. Table 22P shows ON-R2V3vg is PCR amplifiedwith ON-R2top and ON-R2bo3 while ON-R2V4vg is amplified with ON-R2topand ONR2-bo4.

Analysis of HC CDR3:

CDR3s of HC vary in length and in sequence. About half of human HCsconsist of the components: V::nz::D::ny::JHn where V is a V gene, nz isa series of bases (mean 12) that are essentially random, D is a Dsegment, often with heavy editing at both ends, ny is a series of bases(mean 6) that are essentially random, and JH is one of the six JHsegments, often with heavy editing at the 5′ end. In HCs that have noidentifiable D segment, the structure is V::nz::JHn where JH is usuallyedited at the 5′ end. Our goal is to mimic the diversity of CDR3, butnot to duplicate it (which would be impossible). The D segments appearto provide spacer segments that allow folding of the IgG. The greatestdiversity is at the junctions of V with D and of D with JH. The plannedCDR3 library will consist of several components. Some of these will haveonly sequence diversity. Others will have sequence diversity withembedded D segments to extend the length while incorporating sequencesknown to allow Igs to fold.

There are many papers on D segments. Corbett et al. (1997) show which Dsegments are used in which reading frames. My analysis basicallyconfirms their findings. They did not report, however, the level ofediting of each D segment and this information is needed for design ofan effective library.

The following diversified sequences would be incorporated in theindicated proportions: “1” stands for 0.095 [G, Y] and 0.048 [A, D, E,F, H, I, K, L, M, N, P, Q, R, S, T, V, W]; double dose of Gly and Tyrplus all other AAs except Cys at equal level.

The amount of each component is assigned from the tabulation of lengthsof the collection of natural VH genes. Component 1 represents all thegenes having length 0 to 8 (counting from the YYCAR (SEQ ID NO:112)motif to the WG dipeptide motif). Component 2 corresponds the all thechains having length 9 or 10. Component 3 corresponds to the geneshaving length 11 or 12 plus half the genes having length 13. Component 4corresponds to those having length 14 plus half those having length 13.Component 5 corresponds to the genes having length 15 and half of thosehaving length 16. Component 6 corresponds to genes of length 17 plushalf of those with length 16. Component 7 corresponds to those withlength 18. Component 8 corresponds to those having length 19 andgreater.

The composition has been adjusted because the first component is notcomplex enough to justify including it as 10% of the library. If thefinal library were to be 1. E 9, then 1. E 8 sequences would come fromcomponent 1, but it has only 2.6 E 5 CDR3 sequences so that each onewould occur in ˜385 CDR1/2 contexts. I think it better to have thisshort CDR3 diversity occur in ˜77 CDR1/2 contexts and have the other,longer CDR3s occur more often.

The ONs would be PCR amplified with the primers CtprmA and CBprmB, cutwith AflII and BstEII, and ligated to similarly cut V3-23.

This set of components was designed after studying the sequences of 1383human HC sequences as described below. The proposed components are meantto fulfill the goals:

1) approximately the same distribution of lengths as seen in real Abgenes,2) high level of sequence diversity at places having high diversity inreal Ab genes, and3) incorporation of constant sequences often seen in real Ab genes.

Note that the design uses JH4 (YFDYWGQGTLVTVSS; SEQ ID NO:20), which isfound more often, instead of JH3 (AFDIWGQGTMVTVSS; SEQ ID NO:21). Thisinvolves three changes in AA sequence, shown as double underscored bold.An alternative JH segment is shown.

How the Library Components were Designed:

The processing of sequence data was accomplished by a series ofcustom-written FORTRAN programs, each of which carries out a fairlysimple transformation on the data and writes its results as one or moreASCII files. The next program then uses these files as input.

A set of 2049 human heavy-chain genes was selected from the version ofGenBank that was available at Dyax on the Sun server on 26 Jun. 2000. Aprogram named “Reformat” changed the format of the files to that ofGenBank from the GCG format, creating one file per sequence. A secondprogram named “IDENT_CDR3” processed each of these files as follows.Files were tested for duplication by previous entries, duplicates werediscarded. Each reading frame was tested. Most entries had a single openreading frame (ORF), none had two, and some had none. Entries withmultiple stops in every reading frame were discarded because thisindicates poor quality of sequencing. The sequence was written intriplets in the ORF or in all three reading frames if no ORF was found.The sequence was examined for three motifs: a) AA sequence=“YYCxx”, b)DNA sequence=“tgg ggc (=WG)”, and DNA sequence=“g gtc acc (=BstEII)”.FR3 ends with a conserved motif YYCAR or a close approximation. Whenwriting the DNA sequence, IDENT_CDR3 prints the DNA mostly in lowercase. Cysteine codons (TGT or TGC) are printed in uppercase. When themotif “tay tay tgy” is found, IDENT_CDR3 starts a new line that contains“< > xxx xxx xxx xxx xxx” where the xxx's stand for the actual fivecodons that encode YYC and the next two codons (most often AR or AK).The following DNA is printed in triplets on new lines. A typicalprocessed entry appears as in Table 1P.

Following the YYC motif, IDENT_CDR3 seeks the sequence “TGG GGC” (the“WG” motif) in the correct reading frame, 5/6 bases is counted as a hit.If found, the DNA is made uppercase. Following the WG motif (if found)or the YYC motif (if no WG found), IDENT_CDR3 seeks the sequence “G GTCACC” (the BstEII site) in the correct reading frame, 6/7 bases iscounted as a hit. If found, the bases are made upper case. If either theWG or BstEII motif are not found, a note is inserted saying that thefeature was not identified. The output of IDENT_CDR3 was processed byhand. In many cases, the lacking YYC motif could be seen as a closelyrelated sequence, such as YFC, FYC, or HYC. When this was supported byan appropriately positioned WG and/or BstEII site, the effective YYCsite was marked and the sequence retained for further analysis. If theYYC motif could not be identified or if the WG or BstEII sites could notbe found, the entry was discarded. For example, the entry in Table 2Phad no YYC motif.

The double underscored sequence encodes YHCAS and is taken as the end ofFR3. Note that there is a WG motif at bases 403-408 (bold upper case)and a BstEII site at bases 420-426 (bold upper case). Using WordPerfect,I first made all occurrences of TGC and TGT bold. I then searched for“YYC not found”. If I could see the “YYC”-related sequence quickly, Iedited the entry so that a YYC was shown. The entry above would beconverted to that shown in Table 3P. This processing reduced the list ofentries to 1669.

A third program named “New_DJ” processed the output of IDENT_CDR3. Theend of the YYC motif (including the two codon following TGy=Cys) wastaken as the end of FR3. The WG motif was taken as the end of the regionthat might contain a D segment. If WG was not observed and BstEII was,the WG site was assumed to be 17 bases upstream of BstEII. Using the WGmotif for alignment, the sequence was compared to each human GLG JHsegment (1-6) and the best one identified (New_DJ always assigned a JHsegment). Starting from the WG motif of JH and moving toward the 5′ end,the program looked for the first codon having more than one mismatch.The region from YYCxx (SEQ ID NO:113) to this codon was taken as theregion that might contain a D segment.

The region that might contain a D segment was tested against all thegerm-line genes (GLGs) of human D segments and the best D segment wasidentified. The scoring involved matching the observed sequence to theGLG sequence in all possible ways. Starting at each base, multiply by 4for a match and divide by 4 for a mismatch. Record the maximum valueobtained for this function. The match was deemed significant if 7/7,8/9, 9/11, etc. or more bases matched. Of the 1383 sequences examinedfor D segments,

“Assign_D” processes the output of New_DJ. For each sequence that had asignificant match with a GLG D segment, a file was written containingthe putative D segment, the DJ segment, the identified GLG D segment,the identified JH segment, the phase of the match between observed andGLG gene. For example, “D1_(—)1-01_Phz0_hsa239356.txt” is a filerecording the match of entry hsa239356 with D1-01 in phase 0. The filecontains the information shown in Table 4P. The final DV of the secondsequence immediately precedes the WG in JH and is ascribed to JH3. Otherfiles that begin D1_(—)1-01_Phz0 match the same GLG D segment and thesecan be aligned by sliding amino-acid sequences across each other.

Table 5P shows how sequence hs6d4xb7 is first assigned to JH4 and thento D3-22. Note that the DNA sequence TGGGGG is aligned to the TGG GGC ofthe GLG and that the sequence is truncated on the left to fit. Theprogram finds that JH4 has the best fit (5 misses and 18 correct out of23). From the right, the program sees that DYWGQ (underscored) come fromJH, but then the match drops off and the rest of the sequence on theleft comes either from added bases or a D segment.

The lower part of Table 5P shows that the possible D segment matchesD#13 (3-23) is a very good match.

Of 1383 files accepted by Assign_D, 757 had identifiable D segments. Thetally of JHs in Table 6P shows that JH4 is by far the most common.

JH4 is most common, JH6 next, followed by JH3 and JH5. JH1 and JH2 areseldom used. Table 7P shows the length distributions of each JH class;they do not differ significantly class to class. These lengths countonly amino-acids that are not accounted for by JH and so are shorterthat the lengths given in Table 8P which cover from YYCAR (SEQ IDNO:112) to WG.

Table 8P contains the distribution of lengths for a) all the CDR3segments, b) the CDR3 segments with identified D segments, and c) theCDR3 segments having no identifiable D segment. The CDR3s withidentifiable D segments (13.9) are systematically longer than are thosethat lack D segments (11.2).

The identified CDR3 segments can be collated in two ways: aligned to theleft (looking for a pattern following YYCAR; SEQ ID NO:112) or alignedto the right (looking for a pattern preceding WG). Table 9P shows thecollation of left-aligned sequences while Table 10P shows theright-aligned sequences. For each position, I have tabulated thefrequency of each AA type (A-M in the first block and N-Y in thesecond). The column headed “#” shows how many sequences have some AA atthat position. The final column shows all of the AA types seen at thatposition with the most frequent first and the least frequent last. Inthe left-aligned sequences, we see that Gly is highly over-representedin the first seven positions while Tyr is over-represented at positions8-16.

In Table 11P, I have tabulated the AA frequencies for the sequenceshaving between 7 and 15 AAs between YYCAR (SEQ ID NO:112) and WG. Thelast four positions can be viewed as coming from JH and so would begiven lower levels of diversity than would earlier positions. From thesetabulations, I conclude that most AA types are allowed at all thepositions, but there is a fairly strong tendency to have Gly at theearly positions and to end in Asp-Tyr (DY). We could use thesetendencies in designing a pattern of variegation. I would not excludeany AA except Cys, but I might increase the frequency of Gly in thefirst several positions and Tyr in the last few.

There are 80 sequences (5.8%) having a pair of cysteines in CDR3. It ismore surprising that 53 (3.8%) have a single Cys in CDR3.

MS-DOS was used to make a list of the files written by Assign_D.“Filter” converts the output of MS-DOS Dir into a form that can be readinto WordPerfect and sorted to bring a files belonging to the same Dregion together.

“Filter2” collects the sequences and produces a draft table ofsequences, grouped by the D-segment used, and written so that thesequences can be aligned. The output of Filter2 were edited by hand. Foreach group, the translation of the GLG was inserted and the collectionof observed sequences was aligned to the conserved part of the GLG.“Filter3” collated the aligned sequences. Table 12P shows an example ofan alignment and the tabulation of AA types. The entries are as follows:“Entry” is the name used in the data base, “Seq1” is the sequence fromthe YYCAR (SEQ ID NO:112) motif to the first amino acid not assigned toJH and “L1” is the length of the segment. The segments are shown alignedto the identified D segment. Seq2 is the sequence from the YYCAR (SEQ IDNO:112) motif to the WG motif (i.e. including part of JH) and “L2” isthe length of that sequence. JH is the identified JH segment for thissequence. “P” is the phase of the match. For positive values of P, Pbases are found in the observed sequence that do not correspond to anyfrom the GLG, i.e. the observed sequence has had that many basesinserted. For negative values of P, there are |P| bases in the GLGsequence for which there are no corresponding bases in the observedsequence. “Score” is approximately 1/(probability of accidental match).This is calculated by looking at all possible alignments. For eachalignment, the score is first set to 1.0. Base by base, the score ismultiplied by 4. if the bases match and divided by 4. if they do not.This is done for all starting points and ending points and the maximumvalue is recorded.

Table 13P is a summary of how often each D segment was identified and inwhich reading frame. I have not been consistent with Corbett et al. inassigning the phases of the GLG D segments. The MRC Web page that I tookthe GLGs from did not have D segments D1-14, D4-11, D5-18, or D6-25.None of these contribute to any great extent and this omission isunlikely to have any serious effect on the conclusions. The columnheaded “%” contains the percentage of the sequences examined here. Thecolumn headed “C %” contains the percentage reported by Corbett et al. Iassume that the data used in Corbett et al. is mostly included in mycollection. Nevertheless, the observed frequencies differ in detail. Forexample, my compilation shows that 10.7% of the collection contains a Dsegment encoding two cysteines while they have only 4.16% in thiscategory. In D3 phase “0”, I see 19.4% of the collection while theyreport 11.8%.

The most common actual D segments were further analyzed. The GLGs areheavily edited at either end. The aligned sequences were aligned. Foreach D-segment having more than seven examples, Filter3 produced a tableof the frequency of each amino-acid type at each position. From thesetabulations, library components shown in Table 17P were designed. Ateach position where at least half the examples have an amino acid, Ientered either the dominant AA type or “x”. An AA type was “dominant” ifit occurred more than 50% of the time. L is the length and f is thenumber of sequences observed that have related sequences.

Table 14P shows possible library components for a library of CDR3's. “L”is the length of the insert and “f” is the frequency of the motif in theassayed collection. Table 17P shows vgDNA that embodies each of thecomponents shown in Table 14P. In Table 17P, the oligonucleotides (ON)Ctop25, CtprmA, CBprmB, and CBot25 allow PCR amplification of each ofthe variegated ONs (vgDNA): C1t08, C2t10, C3t12, C4t14, C5t15, C6t17,C7t18, and c8t19. After amplification, the dsDNA can be cleaved withAflII and BstEII (or KpnI) and ligated to similarly cleaved vector thatcontains the remainder of the 3-23 synthetic domain. Preferably, thisvector already contains diversity in CDR1 and CDR2 as disclosed herein.Preferably, the recipient vector contains a stuffer in place of CDR3 sothat there will be no parental sequence that would then occur in theresulting library. Table 50P shows a version of the V3-23 gene segmentwith each CDR replaced by a short segment that contains both stop codonsand restriction sites that will allow specific cleavage of any vectorthat does not have the stuffer removed. The stuffer can either be shortand contain a restriction enzyme site that will not occur in the finishlibrary, allowing removal of vectors that are not cleaved by both AflIIand BstEII (or KpnI) and religated. Alternatively, the stuffer could be200-400 bases long so that uncleaved or once cleaved vector can bereadily separated from doubly cleaved vector.

In the vgDNA for HC CDR3, <1> means a mixture comprising 0.27 Y, 0.27 G,and 0.027 of each of the amino-acid codons {A, D, E, F, H, I, K, L, M,N, P, Q, R, S, T, V, W}; <2> means an equimolar mixture of K and R; and<3> means an equimolar mixture of S and G.

Analysis of Human Kappa Light Chains and Preferred Variegation Scheme:

A collection of 285 human kappa chains was assembled from the publicdata base. Table 27 shows the names of the entries used. The GLGsequences of nine bases at each end of the framework regions were usedto find the FR/CDR junctions. Only in cases where all six junctionscould be found was the sequences included. Table 25P shows thedistribution of lengths in CDRs in human kappas. CDR1s with lengths of11, 12, 13, 16, and 17 were observed with 11 being predominant and 12well represented. CDR2 exhibits only length 7. CDR3 exhibits lengths of1, 4, 6, 7, 8, 9, 10, 11, 12, 13, and 19. Essentially all examples arein the 8, 9, or 10 length groups.

Table 26P shows the distribution of V and J genes seen in the sample.A27 is the most common V and JK1 is the most common J. Thus, a suitablesynthetic kappa gene comprises A27 joined to JK1. Table 30P shows asuitable synthetic kappa chain gene, including a PlacZ promoter,ribosome-binding site, and signal sequence (M13 III signal). The DNAsequence encodes the GLG amino-acid sequence, but does not comprise theGLG DNA sequence. Restriction sites are designed to fall within eachframework region so that diversity can be cloned into the CDRs. XmaI andEspI are in FR1, SexAI is in FR2, RsrII is in FR3, and KpnI (or Acc65I)are in FR4. Additional sites are provided in the constant kappa chain tofacilitate construction of the gene.

Table 30P also shows a suitable scheme of variegation for kappa. InCDR1, a preferred length is 11 codons. The A27 GLG has a CDR1 of 12codons, but the sample of mature kappa chains has length 11predominating. One could also introduce a component of kappas havinglength 12 in CDR1 by introducing codon 52 as <2> (i.e. a Ser-biasedmixture). CDR2 of kappa is always 7 codons. Table 31P shows a tally of285 CDR2s and a preferred variegation scheme for CDR2. The predominantlength of CDR3 in kappa chains is 9 codons. Table 32P shows a tally of166 CDR3s from human kappas and a preferred variegation scheme (which isalso shown in Table 30P).

Analysis of Lambda Chains and Preferred Variegation Scheme:

A collection of 158 lambda sequences was obtained from the public database. Of these 93 contained sequences in which the FR/CDR boundariescould be identified automatically. Table 33P shows the distribution oflengths of CDRs.

Method of Construction:

The diversity of HC, kappa, and lambda are best constructed in separatevectors. First a synthetic gene is designed to embody each of thesynthetic variable domains. The light chains are bounded by restrictionsites for ApaLI (positioned at the very end of the signal sequence) andAscI (positioned after the stop codon). The heavy chain is bounded bySfiI (positioned within the PelB signal sequence) and NotI (positionedin the linker between CH1 and the anchor protein. The initial genes aremade with “stuffer” sequences in place of the desired CDRs. A “Stuffer”is a sequence the is to be cut away and replaced by diverse DNA butwhich does not allow expression of a functional antibody gene. Forexample, the stuffer may contain several stop codons and restrictionsites that will not occur in the correct finished library vector. InTable 40P, the stuffer for CDR1 of kappa A27 contains a StuI site. ThevgDNA for CDR1 is introduced as a cassette from EspI, XmaI, or AflII toeither SexAI or KasI. After the ligation, the DNA is cleaved with StuI;there should be no StuI sites in the desired vectors.

REFERENCES

-   Corbett, S J, Tomlinson, I M, Sonnhammer, E L L, Buck, D, Winter, G.    “Sequences of the Human Immunoglobulin Diversity (D) Segment Locus:    A Systematic Analysis Provides No Evidence for the Use of DIR    Segments, Inverted D Segments, ‘Minor’ D Segments or D-D    Recombination”. J Molec Biol (1997) 270:587-597.

Tables

TABLE 1P  Typical entry in which YYC motif is found.++++C:\tmp\haj10335.txt LOCUS HAJ10335 306 bp mRNA PRI 18 AUG. 1998DEFINITION Homo sapiens mRNA for immunoglobulin heavy chainvariable region, clone ELD16/6. ACCESSION AJ010335 VERSIONAJ010335.1 GI:3445266 Ngene = 306 Stop codons in reading frame 1   49 115 124 253 277 No stops in reading frame 2Stop codons in reading frame 3    12  60  81 147 204 213  1   t ttg ggg tcc ctg aga ctc tcc TGT gca gcc tct gga ttc acc 44 gtc agt agc aac tac atg acc tgg gtc cgc cag gct cta ggg aag 89 ggg ctg gag tgg gtc tca gtt att tat agc ggt ggt agc aca tac134 tac gca gac tcc gtg aag ggc gga ttc acc atc tcc aga gac aat179 tcc aag aac aca ctg tat ctt caa atg aac agc ctg aga ccc gag224 gac acg gct gtg <     > TAT TAC TGT gcg aca251 ggt aat cgc ctg gaa atg gct gca att aac TGG GGC caa gga acc263 ctG GTC ACC aa (SEQ ID NO: 113)

TABLE 2P  entry in which YYC motif was not automatically identified++C:\tmp\hs202g3.txt !!NA_SEQUENCE 1.0 LOCUSHS202G3 522 bp mRNA PRI 03 AUG. 1995 DEFINITIONH. sapiens mRNA for immunoglobulin variable region (clone 202-G3).ACCESSION Z47259 VERSION Z47259.1 GI:619470 Ngene = 522No stops in reading frame 1 Stop codons in reading frame 2   89 110 305 314 Stop codons in reading frame 3    84 192 321 351 369  1 atg gac tgg acc tgg agg ttc ctc ttt gtg gtg gca gca gct aca 46 ggt gtc cag tcc cag gtg cag ctg gtg cag tct ggg gct gag gtg 91 aag aag cct ggg tcc tcg gtg aag gtc tcc TGC aag gct tct gga136 ggc acc ttc agc agc tat gct atc agc tgg gtg cga cag gcc cct181 gga caa ggg ctt gag tgg atg gga ggg atc atc cct atc ttt ggt226 aca gca aac tac gca cag aag ttc cag ggc aga gtc acg att acc271 gcg gac gaa tcc acg agc aca gcc tac atg gag ctg agc agc ctg316 aga tct gag gac acg gcc gtg tat cac TGT gcg agt gag gga tgg361 gag agt TGT agt ggt ggt ggc TGC tac gac ggt atg gac gtc TGG406 GGC caa ggg acc acG GTC ACC gtc tcc tca gct tcc acc aag ggc451 cca tcg gtc ttc ccc ctg gcg ccc TGC tcc agg agc acc tct ggg496 ggc aca gcg gcc ctg ggc TGC ctg (SEQ ID NO: 114) YYC not found !!!

TABLE 3P  Entry of Table 2P after editting. ++C:\tmp\hs202g3.txt!!NA SEQUENCE 1.0 LOCUS HS202G3 522 bp mRNA PRI 03 AUG. 1995 DEFINITIONH. sapiens mRNA for immunoglobulin variable region (clone 202-G3).ACCESSION 247259 VERSION 247259.1 GI:619470 Ngene = 522No stops in reading frame 1 Stop codons in reading frame 2   89 110 305 314 Stop codons in reading frame 3    84 192 321 351 369  1 atg gac tgg acc tgg agg ttc ctc ttt gtg gtg gca gca gct aca 46 ggt gtc cag tcc cag gtg cag ctg gtg cag tct ggg gct gag gtg 91 aag aag cct ggg tcc tcg gtg aag gtc tcc TGC aag gct tct gga136 ggc acc ttc agc agc tat gct atc agc tgg gtg cga cag gcc cct181 gga caa ggg ctt gag tgg atg gga ggg atc atc cct atc ttt ggt226 aca gca aac tac gca cag aag ttc cag ggc aga gtc acg att acc271 gcg gac gaa tcc acg agc aca gcc tac atg gag ctg agc agc ctg316 aga tct gag gac acg gcc gtg  <YHCAS> tat cac TGT gcg agt(SEQ ID NO: 116)     gag gga tgg361 gag agt TGT agt ggt ggt ggc TGC tac gac ggt atg gac gtc TGG406 GGC caa ggg acc acG GTC ACC gtc tcc tca gct tcc acc aag ggc451 cca tcg gtc ttc ccc ctg gcg ccc TGC tcc agg agc acc tct ggg496 ggc aca gcg gcc ctg ggc TGC ctg (SEQ ID NO: 115) YYC not found !!!

TABLE 4P  contents of file D1_1-01_Phz0_hsa239356.txtDRGGKYQLAPKGGM (SEQ ID NO: 117) DRGGKYQLAPKGGMDV (SEQ ID NO: 118)JH3 D#1 Phase 15 Score 6.55D+04

TABLE 5P  alignment of a CDR3::JH segment to GLG JHs and D-segments.+C:\tmp\hs6d4xb7.txt          1    1    2   2     3    3   31234567890    5    0   5     0    5   9 ObservedtatgatagtagtgggtcatactccgactacTGGGGGcag (SEQ ID NO: 119) JH1------------gctgaatacttccagcactggggccagggcaccctggtcaccgtctcctcag--Miss = 9 Nt = 27 (SEQ ID NO: 120) JH2-----------ctactggtacttcgatctctggggccgtggcaccctggtcactgtctcctcag--Miss = 13 Nt = 28 (SEQ ID NO: 121) JH3--------------tgatgcttttgatatctggggccaagggacaatggtcaccgtctcttcag--Miss = 14 Nt = 25 (SEQ ID NO: 122) JH4----------------actactttgactactggggccagggaaccctggtcaccgtctcctcag--Miss = 5 Nt = 23 (SEQ ID NO: 123) JH5-------------acaactggttcgacccctggggccagggaaccctggtcaccgtctcctcag--Miss = 11 Nt = 26 (SEQ ID NO: 124) JH6-attactactactactacggtatggacgtctggggccaagggaccacggtcaccgtctcctcag--Miss = 23 Nt = 38 (SEQ ID NO: 125)   4tat gat agt agt ggg tca TAC Tcc GAC TAC TGG GGg CAG (SEQ ID NO: 126)Y D S S G S Y S D Y W G Q (SEQ ID NO: 127) JH4--- --- --- --- --- -ac tac ttt gac tac tgg ggc cag gga acc ctg gtc acc gtc tcc tca g--(SEQ ID NO: 128) -   -   -   -   -   -   Y   F   D   Y   W   G   Q   G   T   L   V   T   V   S   S   -(SEQ ID NO: 129) Fract = 0.783 = 18/23 Matching the rest to D segments:D#13 --------gtattactatgatagtagtggttattactac GLG      (SEQ ID NO: 130)     gatcgccacaattactatgatagtagtgggtcatactcc Observed (SEQ ID NO: 131)     --------gt...................t.at....a. . = match D#13 Phase =9 Score = 4.3980E+12

TABLE 6P Number of sequences identified as having JH derived from GLGJHn JH 1 2 3 4 5 6 # sequences 17 40 198 707 160 261

TABLE 7P Distribution of CDR3 fragments that might contain D segments.For JH1 0 1 2 3 4 5 6 7 8 9 10 11 12 13 0 0 1 1 3 1 1 2 0 3 1 1 1 2Total = 17 Median = 8.0 For JH2 0 1 2 3 4 5 6 7 8 9 10 11 12 13 14 0 0 00 0 2 4 6 2 6 3 4 5 2 3 15 16 17 18 2 0 0 1 Total = 40 Median = 9.0 ForJH3 0 1 2 3 4 5 6 7 8 9 10 11 12 13 14 0 0 2 6 16 12 17 17 15 22 20 2018 13 4 15 16 17 18 19 8 3 2 1 2 Total = 198 Median = 8.6 For JH4 0 1 23 4 5 6 7 8 9 10 11 12 13 14 0 0 7 15 19 40 63 82 81 77 81 53 57 44 3015 16 17 18 19 20 21 22 23 24 25 26 27 28 29 15 23 8 3 5 2 0 1 0 0 0 0 00 0 30 31 32 33 34 35 0 0 0 0 0 1 Total = 707 Median = 8.6 For JH5 0 1 23 4 5 6 7 8 9 10 11 12 13 14 0 0 0 3 4 6 13 19 12 14 22 18 10 18 10 1516 17 18 19 20 21 22 23 24 25 26 27 28 29 5 1 1 0 0 1 1 0 0 0 0 0 0 0 030 31 32 33 34 35 36 37 38 39 40 41 42 43 44 0 0 0 0 0 0 0 0 0 0 0 0 1 00 45 46 0 1 Total = 160 Median = 9.4 For JH6 0 1 2 3 4 5 6 7 8 9 10 1112 13 14 2 0 1 2 5 15 20 18 22 29 29 28 23 16 10 15 16 17 18 19 20 14 99 4 2 3 Total = 261 Median = 9.6

TABLE 8P Lengths of CDR3 segments from YYCAR to WG. Distribution oflengths from end of FR3 to WG motif all sequences. L 0 1 2 3 4 5 6 7 8 910 11 12 13 14 N 6 0 0  4  2  9 13 38  61  88 101 118 154 150 118 Sum(N)6 6 6 10 12 21 34 72 133 221 322 440 594 744 862 f .004 .004 .004 .007.009 .015 .025 .052 .096 .160 .233 .318 .430 .538 .623 L 15 16 17 18 1920 21 22 23 24 25 26 27 28 29 N 125  105  84  61  46  42  16  17   7   9  2   1   0   2   1 SN 987 1092 1176 1237 1283 1325 1341 1358 1365 13741376 1377 1377 1379 1380 f .714 .790 .850 .894 .928 .958 .970 .982 .987.993 .995 .996 .996 .997 .998 L 30 31 32 33 34 35 36 37 38 39 40 41 4243 44 N   0   0   0   0   0   0   0   1   0   0   0   0   1   0   0 SN1380 1380 1380 1380 1380 1380 1380 1381 1381 1381 1381 1381 1382 13821382 f .998 .998 .998 .998 .998 .998 .998 .999 .999 .999 .999 .999 .999.999 .999 L 45 46 N   0   1 SN 1382 1383 f .999 1.0 Median = 12.65Distribution of lengths from end of FR3 to WG motif with assigned D. L 01 2 3 4 5 6 7 8 9 10 11 12 13 14 N 3 0 0 0 0 0 3  9 21 15 39  64  77  97 72 SN 3 3 3 3 3 3 6 15 36 51 90 154 231 328 400 f .004 .004 .004 .004.004 .004 .008 .019 .046 .065 .115 .196 .294 .418 .510 L 15 16 17 18 1920 21 22 23 24 25 26 27 28 29 N  77  75  63  45  35  38  15  15  6  9  2 1  0  1  1 SN 477 552 615 660 695 733 748 763 769 778 780 781 781 782783 f .608 .703 .783 .841 .885 .934 .953 .972 .980 .991 .994 .995 .995.996 .997 L 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 N  0  0  0  0 0  0  0  1  0  0  0  0  0  0  0 SN 783 783 783 783 783 783 783 784 784784 784 784 784 784 784 f .997 .997 .997 .997 .997 .997 .997 .999 .999.999 .999 .999 .999 .999 .999 L 45 46 N  0  1 SN 784 785 f .999 1.0Median = 13.90 Distribution of lengths from end of FR3 to WG motif withno assigned D. L 0 1 2 3 4 5 6 7 8 9 10 11 12 13 14 N 3 0 0 4 2  9 10 2940  73  62  54  77  53  46 SN 3 3 3 7 9 18 28 57 97 170 232 286 363 416462 f .005 .005 .005 .012 .015 .030 .047 .095 .162 .284 .388 .478 .607.696 .773 L 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 N  48  30  21 16  11  4  1  2  1  0  0  0  0  1  0 SN 510 540 561 577 588 592 593 595596 596 596 596 596 597 597 f .853 .903 .938 .965 .983 .990 .992 .995.997 .997 .997 .997 .997 .998 .998 L 30 31 32 33 34 35 36 37 38 39 40 4142 N  0  0  0  0  0  0  0  0  0  0  0  0  1 SN 597 597 597 597 597 597597 597 597 597 597 597 598 f .998 .998 .998 .998 .998 .998 .998 .998.998 .998 .998 .998 1.0 Median = 11.17 L is the length N is the numberof examples Sum(N) = SN is the sum of the Ns f is the cumulativefraction seen

TABLE 9P  Tally of left-aligned CDR3 sequences A C D E F G H I K L M # 174 6 278 109 11 319 50 18 11 60 8 1383 GDERVASLHTNQPIWYFKMCX 2 50 9 6432 29 249 43 42 41 109 22 1377 GRPSLDVYTANHIQKEFMWCX 3 81 18 74 39 25214 29 42 16 83 19 1377 GSYRTVLADPIWEQHNFMCK| 4 70 23 92 49 50 228 23 5821 70 16 1373 GSYDRVALTIPFEWNCHQKMX 5 86 28 106 32 59 217 21 41 16 72 191371 GYSDAVTLRFIPWNECHMQK|X 6 88 17 104 28 94 171 17 48 12 50 17 1362GYSDFATVRWPLINEQCHMK| 7 69 15 110 21 89 176 22 50 15 81 12 1349GSYDFVLTAPRWINHEQCKM|X 8 53 19 141 17 90 150 18 47 17 68 11 1311YSGDFLTVWAPIRNCHEKQM| 9 44 21 120 24 102 174 24 36 20 71 11 1250YGSDFLNVRTAWPIEHCKQM| 10 39 31 129 23 124 116 23 42 9 58 32 1162YDFGSLIARPTVWNMCEHQK 11 36 12 158 17 137 83 13 18 10 40 21 1061YDFGSPLVANWMTRIEHCKQX 12 34 11 164 10 82 74 34 30 1 31 20 943YDFGPSVAHLINMRTWCEQKX 13 32 2 121 6 84 56 10 26 7 43 32 789YDFGLSPVAMIWRTHNKQEC 14 23 131 5 59 65 10 16 4 25 34 639YDGFMVLAPISWNRHTQEKX 15 15 4 107 5 43 42 1 23 20 34 521YDFGVMILWAPRSENCQTH| 16 4 2 80 3 33 26 4 5 1 10 29 396YDVFMGPSLNTRIWAHECQ|K 17 3 1 63 19 19 9 13 12 21 291 DYVMFGILHPSTWAQRCNX18 3 47 16 13 1 4 7 23 207 DYVMFGPSLTIAHN 19 5 1 39 1 4 13 3 3 1 14 146DYVMGAFHINRSCELPQW 20 2 17 4 5 3 4 12 100 VYDMGFLIPSARWQ 21 17 3 8 1 1 458 DVGYMFHINTW 22 1 7 6 1 1 5 42 VDFMYSAGITW 23 9 1 1 1 1 25 DVYGILMPS24 1 2 1 1 1 18 VYDAHLMPT 25 1 3 9 GVDPSY 26 2 2 7 GMSTV 27 2 1 1 6DKMST 28 1 1 1 6 VADGS 29 1 4 DPSV 30 1 3 FST 31 1 1 3 KLV 32 1 1 3 FGP33 1 3 PG 34 1 1 3 HLS 35 1 3 AVW 36 1 1 3 DFP 37 3 PSY 38 1 2 LS 39 1 12 AK 40 2 PS 41 2 ST 42 2 S 43 1 1 K 44 1 S 45 1 T 46 1 S 816 220 2186421 1166 2428 358 568 205 920 421 N P Q R S T V W Y | X # 1 35 23 31 10863 50 94 16 13 6 1383 GDERVASLHTNQPIWYFKMCX 2 44 114 42 169 114 59 62 2160 2 1377 GRPSLDVYTANHIQKEFMWCX 3 26 73 37 110 140 97 89 42 122 1 1377GSYRTVLADPIWEQHNFMCK| 4 48 51 22 79 141 65 77 49 139 2 1373GSYDRVALTIPFEWNCHQKMX 5 37 41 18 61 157 75 85 38 158 2 2 1371GYSDAVTLRFIPWNECHMQK|X 6 32 54 23 67 152 80 78 64 165 1 1362GYSDFATVRWPLINEQCHMK| 7 44 59 18 58 157 73 85 54 139 1 1 1349GSYDFVLTAPRWINHEQCKM|X 8 38 48 14 41 167 68 59 59 185 1 1311YSGDFLTVWAPIRNCHEKQM| 9 52 40 14 47 123 45 48 41 192 1 1250YGSDFLNVRTAWPIEHCKQM| 10 33 37 12 39 73 36 36 35 235 1162YDFGSLIARPTVWNMCEHQK 11 33 49 7 20 68 21 37 29 251 1 1061YDFGSPLVANWMTRIEHCKQX 12 30 53 10 19 45 19 42 18 215 1 943YDFGPSVAHLINMRTWCEQKX 13 10 34 7 22 40 15 33 25 184 789YDFGLSPVAMIWRTHNKQEC 14 13 22 6 12 15 10 26 14 148 1 639YDGFMVLAPISWNRHTQEKX 15 5 12 3 12 12 3 40 20 119 1 521YDFGVMILWAPRSENCQTH| 16 10 24 2 6 12 7 49 5 82 2 396YDVFMGPSLNTRIWAHECQ|K 17 1 8 2 2 8 5 42 4 58 1 291 DYVMFGILHPSTWAQRCNX18 1 13 8 5 31 35 207 DYVMFGPSLTIAHN 19 2 1 1 2 2 24 1 29 146DYVMGAFHINRSCELPQW 20 3 1 2 3 23 2 19 100 VYDMGFLIPSARWQ 21 1 1 14 1 758 DVGYMFHINTW 22 2 1 12 1 5 42 VDFMYSAGITW 23 1 1 5 5 25 DVYGILMPS 24 11 5 5 18 VYDAHLMPT 25 1 1 2 1 9 GVDPSY 26 1 1 1 7 GMSTV 27 1 1 6 DKMST28 1 2 6 VADGS 29 1 1 1 4 DPSV 30 1 1 3 FST 31 1 3 KLV 32 1 3 FGP 33 2 3PG 34 1 3 HLS 35 1 1 3 AVW 36 1 3 DFP 37 1 1 1 3 PSY 38 1 2 LS 39 2 AK40 1 1 2 PS 41 1 1 2 ST 42 2 2 S 43 1 K 44 1 1 S 45 1 1 T 46 1 1 S 495769 270 876 1518 741 1104 540 2572 10 17 18621

TABLE 10P  Tally of right-aligned sequences A C D E F G H I K L M # 5 11 G 6 1 S 7 1 1 G 8 1 1 G 9 2 RV 10 2 RV 11 1 1 2 GI 12 2 V 13 2 TY 14 11 3 DGN 15 1 3 ISY 16 1 3 DSY 17 1 3 APY 18 1 1 1 3 DFM 19 2 1 3 DG 20 11 3 ILV 21 3 WP 22 3 4 GS 23 2 1 6 GHQSV 24 1 3 1 6 GALR 25 1 2 1 7DTAIS 26 1 1 1 1 1 1 1 9 ACDGKLMST 27 2 5 1 2 1 1 18 DAGVEILNQRS 28 2 23 1 2 25 TGQSDELPRIV 29 3 5 6 7 1 1 1 42 GEDVAPQRSKLMTY| 30 2 9 1 9 1 45 2 58 DGRLSIVPAMQTFHNY 31 4 2 19 9 2 18 1 2 1 3 100 DGSERVYALPTCFINHKW32 10 5 18 5 3 16 3 3 2 14 1 146 DGLRVAPYSTCEQFHINWKM 33 20 18 10 7 34 78 2 9 1 207 GARDPSYTEVIFHLQWKM 34 13 4 31 18 9 37 8 16 4 14 4 291GDRYPVEILASTFHQWCKMNX| 35 17 5 32 23 10 70 12 10 6 25 1 396GRSDYLEVTPAHNFIWKCQM| 36 23 6 51 21 9 79 19 15 14 36 9 521GDSYRLTVPAEHIKNFMWCQ| 37 35 12 56 23 15 110 14 17 5 24 4 639GYDVRSTAPLEIFHNCWQKMX 38 28 19 68 27 29 133 26 31 12 43 7 789GSYDVRLPTIFAEHCNWKQM 39 51 25 80 27 33 162 16 30 18 55 15 943GSDRYVLATPFWIECKHMQNX 40 44 14 73 36 46 161 27 32 17 59 8 1061GSRDYVTLPFAEIWHQNKCM 41 54 21 74 25 23 178 23 52 15 57 11 1162GSYTDRVLPAIWNQEFHCKMX| 42 57 13 82 40 42 190 14 39 15 82 15 1250GSYDLVRTANPFEIWQKMHC| 43 75 18 54 25 35 242 13 29 18 49 12 1311GYSTARVPDLWNFIQECKHM| 44 63 17 79 15 43 197 20 38 14 76 8 1349YGSTDLRAPVWNFIQHCEKM 45 59 16 69 35 55 165 26 23 23 75 9 1362YGSLRTDNAFPVWEHIKCQM 46 41 19 125 26 27 208 31 14 16 38 8 1371YGDSNRWATLPHFEVQCKIM 47 160 10 24 13 53 332 36 16 11 40 10 1373GYAWPSFRLHTVNDIEKCMQX 48 21 4 8 5 680 27 4 44 5 145 288 1377FMLISGVYPAWTDNQREKCHX 49 23 2 1181 29 1 30 15 4 2 8 1 1377DGEAHNQSYVLPTIRCKW|FMX 50 7 7 15 42 3 41 135 3 59 4 1383YVIPSLFHNDTACXMGKQRW| 816 220 2186 421 1166 2428 358 568 205 920 421 N PQ R S T V W Y | X # 5 1 G 6 1 1 S 7 1 G 8 1 G 9 1 1 2 RV 10 1 1 2 RV 112 GI 12 2 2 V 13 1 1 2 TY 14 1 3 DGN 15 1 1 3 ISY 16 1 1 3 DSY 17 1 1 3APY 18 3 DFM 19 3 DG 20 1 3 ILV 21 1 2 3 WP 22 1 4 GS 23 1 1 1 6 GHQSV24 1 6 GALR 25 1 2 7 DTAIS 26 1 1 9 ACDGKLMST 27 1 1 1 1 2 18DAGVEILNQRS 28 2 3 2 3 4 1 25 TGQSDELPRIV 29 3 3 2 2 1 5 1 1 42GEDVAPQRSKLMTY| 30 1 3 2 7 5 2 4 1 58 DGRLSIVPAMQTFHNY 31 2 3 7 10 3 7 16 100 DGSERVYALPTCFINHKW 32 3 9 4 12 8 6 12 3 9 146 DGLRVAPYSTCEQFHINWKM33 16 6 19 15 12 10 3 13 207 GARDPSYTEVIFHLQWKM 34 2 20 5 31 12 12 20 523 1 2 291 GDRYPVEILASTFHQWCKMNX| 35 12 18 5 39 35 19 23 7 26 1 396GRSDYLEVTPAHNFIWKCQM| 36 11 24 6 42 47 29 28 7 44 1 521GDSYRLTVPAEHIKNFMWCQ| 37 14 33 9 54 52 37 55 11 58 1 639GYDVRSTAPLEIFHNCWQKMX 38 18 33 12 46 77 32 58 17 73 789GSYDVRLPTIFAEHCNWKQM 39 11 38 12 70 94 42 61 33 68 2 943GS DRYVLATPFWIECKHMQNX 40 24 52 27 74 140 61 66 29 71 1061GSRDYVTLPFAEIWHQNKCM 41 31 55 29 70 156 76 61 51 97 1 2 1162GSYTDRVLPAIWNQEFHCKMX| 42 48 47 24 68 171 68 70 39 125 1 1250GSYDLVRTANPFEIWQKMHC| 43 38 58 28 73 164 76 66 43 194 1 1311GYSTARVPDLWNFIQECKHM| 44 48 60 24 69 131 86 57 52 252 1349YGSTDLRAPVWNFIQHCEKM 45 62 51 16 75 116 74 50 39 324 1362YGSLRTDNAFPVWEHIKCQM 46 97 38 21 55 110 39 26 55 377 1371YGDSNRWATLPHFEVQCKIM 47 25 54 9 44 54 34 32 122 292 2 1373GYAWPSFRLHTVNDIEKCMQX 48 8 22 7 6 28 10 25 16 23 1 1377FMLISGVYPAWTDNQREKCHX 49 15 6 13 4 13 5 9 2 11 2 1 1377DGEAHNQSYVLPTIRCKW|FMX 50 23 122 3 3 67 9 350 3 480 1 6 1383YVIPSLFHNDTACXMGKQRW| 50 495 769 270 876 1518 741 1104 540 2572 10 1718621

TABLE 11P  Tallies of AA frequencies in all CDR3 by lengthTally of sequences of length 7 # = 38 A C D E F G H I K L M # 1 1 8 1 114 1 1 5 38 GDLRWAEFHKS 2 1 1 2 6 3 2 1 1 38 RGNHVFKTYADLMW 3 1 4 1 5 12 2 38 GSDWYPVILTAFHN 4 3 1 1 12 1 1 1 38 GYSANRVDFHILPT 5 2 1 14 3 4 13 3 38 FIGLMARVYEKP 6 26 1 1 38 DVPTHISWY 7 1 2 2 3 1 38 YVINDHSALR 9 422 19 40 9 11 4 13 4 N P Q R S T V W Y | X # 1 3 1 2 38 GDLRWAEFHKS 2 6 72 3 1 2 38 RGNHVFKTYADLMW 3 1 3 5 2 3 4 4 38 GSDWYPVILTAFHN 4 2 1 2 4 12 6 38 GYSANRVDFHILPT 5 1 2 2 2 38 FIGLMARVYEKP 6 2 1 2 3 1 1 38DVPTHISWY 7 3 1 2 7 16 38 YVINDHSALR 12 7 15 13 7 20 8 31 266Tally of sequences of length 8 # = 61 A C D E F G H I K L M # 1 3 7 3 142 2 5 61 GDLTVRSAEHINWPQY 2 1 9 1 1 15 1 2 1 61 GDTNRSVKWYAEFILPQ 3 2 31 10 1 1 7 1 61 GLSTYVDPRAFHIMNQW 4 4 1 3 1 1 15 1 4 61GYRALQDSWVCEFHNPT 5 10 2 1 9 5 1 5 1 61 AGYHLTPRVDSEKMW 6 5 1 24 2 7 5 261 FIALPSVYGMCQRW 7 5 37 2 4 1 2 61 DAHSELNVIP| 8 1 2 3 1 12 3 61YISFLVDNAHPRT 31 2 63 8 30 65 14 24 3 32 4 N P Q R S T V W Y | X # 1 2 11 4 4 5 5 2 1 61 GDLTVRSAEHINWPQY 2 6 1 1 4 3 8 3 2 2 61GDTNRSVKWYAEF I LPQ 3 1 3 1 3 7 7 5 1 7 61 GLSTYVDPRAFHIMNQW 4 1 1 4 5 31 2 3 11 61 GYRALQDSWVCEFHNPT 5 4 4 2 5 4 1 7 61 AGYHLTPRVDSEKMW 6 3 1 13 3 1 3 61 FIALPSVYGMCQRW 7 2 1 4 2 1 61 DAHSELNVIPI 8 2 1 1 7 1 3 24 61YISFLVDNAHPRT 14 15 8 22 33 27 27 10 55 1 488Tally of sequences of length 9 # = 88 A C D E F G H I K L M # 1 9 12 421 1 1 2 5 88 GDARNVLEQTKWHIPSY 2 2 2 3 3 13 4 3 7 2 88GPSRLNTHEFKYADMQW 3 4 2 3 3 3 15 1 1 88 GTPSQNRVWYADEFCLM 4 5 1 6 3 6 222 4 1 6 1 88 GSDFLARITYENPWHVCKM 5 7 1 4 3 4 14 2 7 2 88GSYALNDFVERWHMQTCP 6 13 2 1 3 13 6 2 1 4 1 88 YAGHNLPSVFTWDIEKMQR 7 4 241 2 3 1 14 5 88 FLMAPWIDGSVKNQTY 8 1 1 73 2 2 1 2 88 DEGLSACHNQRV 9 1 14 1 3 8 2 88 YVISFHPLNTCDGR 45 6 105 19 64 103 19 18 8 48 12 N P Q R S TV W Y | X # 1 7 1 3 8 1 3 7 2 1 88 GDARNVLEQTKWHIPSY 2 5 11 2 10 11 5 23 88 GPSRLNTHEFKYADMQW 3 5 7 6 5 7 11 5 5 5 88 GTPSQNRVWYADEFCLM 4 3 3 57 4 2 3 4 88 GSDFLARITYENPWHVCKM 5 6 1 2 3 12 2 4 3 11 88GSYALNDFVERWHMQTCP 6 5 4 1 1 4 3 4 3 17 88 YAGHNLPSVFTWDIEKMQR 7 1 4 1 21 2 4 1 88 FLMAPWIDGSVKNQTY 8 1 1 1 2 1 88 DEGLSACHNQRV 9 2 3 1 8 2 9 4388 YVISFHPLNTCDGR 35 34 16 34 54 31 34 22 85 792Tally of sequences of length 10 # = 101 A C D E F G H I K L M # 1 8 1 197 1 16 3 2 3 2 101 DGNAERTSQVHLWKMYCF 2 3 8 3 5 13 5 15 2 101LGRDSPVFINTAEQYMW 3 6 9 1 26 1 3 1 4 1 101 GSYDAVTLNRIPWFHKMQ 4 7 6 1 251 5 4 1 101 GSYARDINPLTVWQFHM 5 6 5 9 4 16 1 3 4 101 GYTESANDPRFLVKQWH 66 1 6 5 4 23 2 4 3 3 1 101 GYRSWADEFINKLTHCMQV 7 13 3 1 5 9 3 1 4 1 101YASGPRWFTVLDHNEIMQ 8 2 1 1 57 3 4 15 4 101 FLIMSGWANPVCEY 9 3 78 2 6 1 11 101 DGAQENIKLPRSW 10 3 4 4 13 1 101 YIPSVFHNDL 54 3 137 28 82 137 1536 10 54 12 N P Q R S T V W Y | X # 1 9 4 6 5 6 4 3 2 101DGNAERTSQVHLWKMYCF 2 5 6 3 11 8 4 6 1 3 101 LGRDSPVFINTAEQYMW 3 4 3 1 414 5 6 2 10 101 GSYDAVTLNRIPWFHKMQ 4 5 5 3 7 11 4 4 4 8 101GSYARDINPLTVWQFHM 5 6 5 2 5 8 10 4 2 11 101 GYTESANDPRFLVKQWH 6 4 1 8 73 1 7 12 101 GYRSWADEFINKLTHCMQV 7 2 7 1 7 11 5 5 6 17 101YASGPRWFTVLDHNEIMQ 8 2 2 4 2 3 1 101 FLIMSGWANPVCEY 9 2 1 3 1 1 1 101DGAQENIKLPRSW 10 4 8 7 5 52 101 YIPSVFHNDL 43 37 18 49 76 37 37 29 1161010 Tally of sequences of length 11 # = 118 A C D E F G H I K L M # 1 71 21 11 23 5 2 7 118 GDEVRALQHSPTINCWY 2 1 2 9 1 1 24 5 6 2 7 3 118GSRDYLPIVHQTMNCKWAEFX 3 4 4 2 4 13 2 3 1 7 2 118 SGTVRLYWADFNQIEHMKP 410 3 3 2 25 1 2 4 3 118 SGARTWYLVDEMQFINPH 5 5 2 10 1 4 24 2 1 5 1 118GSVYDTNALRFWCHQEKM 6 6 4 2 7 19 2 3 1 5 1 118 GSYWTFAVLRDINEHQKMP 7 4 18 5 2 20 4 1 2 1 118 GYSNRDWTEPAHFLQVCIM 8 13 2 6 1 8 12 4 2 7 118YAGWFLDPRSTHCKVE 9 2 2 68 2 5 14 7 118 FLMYVITADGP 10 2 1 100 5 3 2 1 1118 DEGAHCLMNPQ 11 2 6 1 7 1 6 1 118 YPVISFLNDHKM 54 9 169 31 102 165 2829 8 65 20 N P Q R S T V W Y | X # 1 2 4 7 8 5 3 10 1 1 118GDEVRALQHSPTINCWY 2 3 7 4 10 11 4 6 2 9 1 118 GSRDYLPIVHQTMNCKWAEFX 3 41 4 8 25 12 9 6 7 118 SGTVRLYWADFNQIEHMKP 4 2 2 3 9 26 8 4 6 5 118SGARTWYLVDEMQFINPH 5 6 2 5 15 9 11 4 11 118 GSVYDTNALRFWCHQEKM 6 3 1 2 516 9 6 11 15 118 GSYWTFAVLRDINEHQKMP 7 9 5 2 9 11 6 2 7 19 118GYSNRDWTEPAHFLQVCIM 8 6 5 5 5 2 11 29 118 YAGWFLDPRSTHCKVE 9 1 4 6 7 118FLMYVITADGP 10 1 1 1 118 DEGAHCLMNPQ 11 3 13 7 11 60 118 YPVISFLNDHKM 3341 25 59 121 60 67 48 163 1 1298 Tally of sequences of length 12 # = 154A C D E F G H I K L M # 1 5 31 12 37 6 1 1 7 3 154 GDRESVLHAPMNQTWYIK 25 1 7 6 1 25 3 7 3 13 2 154 GSRLPDIQEAVYHKNTMWCF 3 10 2 7 5 1 19 5 4 122 154 GRSYLATVPDQEIKWCMNF 4 8 9 6 8 27 6 5 6 1 154 GVSDNAFRTYEILKWPQM 518 1 8 5 6 42 1 9 1 7 3 154 GSAIDYLFPTEQVMNWCHK 6 13 12 4 10 23 1 7 8 1154 GAVDSFYTLPRWINEQHM 7 11 2 4 3 10 15 1 4 12 154 YGSPLRAFWTNVDIECQH 83 2 18 3 3 25 4 2 5 6 154 YGDSNLTKRWHPAEFCIQV 9 15 1 2 8 33 4 7 1 5 1154 GYWARFISPLHTDQCKMN 10 1 1 2 1 79 1 2 5 1 19 26 154FMLIPYDHVWACEGKNQRST 11 2 135 2 4 2 154 DGYAEHSVNR 12 1 1 6 1 9 16 4 154YVPIHFSLNCDGW 91 11 236 47 132 252 33 69 21 99 39 N P Q R S T V W Y | X# 1 3 4 3 14 10 3 10 2 2 154 GDRESVLHAPMNQTWYIK 2 3 11 7 22 24 3 5 2 4154 GSRLPDIQEAVYHKNTMWCF 3 2 8 6 17 17 9 9 4 15 154 GRSYLATVPDQEIKWCMNF4 9 4 4 7 17 7 18 5 7 154 GVSDNAFRTYEILKWPQM 5 3 6 4 20 6 4 2 8 154GSAIDYLFPTEQVMNWCHK 6 5 8 3 8 11 9 13 8 10 154 GAVDSFYTLPRWINEQHM 7 5 142 12 15 6 5 9 24 154 YGSPLRAFWTNVDIECQH 8 10 4 2 5 15 6 2 5 34 154YGDSNLTKRWHPAEFCIQV 9 1 6 2 10 7 3 18 30 154 GYWARFISPLHTDQCKMN 10 1 4 11 1 1 2 2 3 154 FMLIPYDHVWACEGKNQRST 11 1 1 2 2 3 154 DGYAEHSVNR 12 2 185 32 1 58 154 YVPIHFSLNCDGW 45 87 34 97 144 53 102 58 198Tally of sequences of length 13 # = 150 A C D E F G H I K L M # 1 4 2 289 3 37 8 3 3 5 150 GDTESHRVLPAQFIKCNW 2 11 4 4 1 2 32 3 1 5 11 3 150GRSPALTKVCDYHMQWFEIN 3 7 2 8 4 4 23 11 1 4 6 2 150 GSYHQTDPRAVLEFKNCMWI4 6 2 6 4 6 30 1 8 6 1 150 GSWYTIADFLPVEQRCHMNX 5 8 10 4 2 28 1 2 22 3150 GLSYDATWPREQMNVFIH 6 10 2 11 1 6 21 2 2 5 1 150 GYSPTDAQVFRLNWCIKEM7 5 1 8 1 4 19 1 6 5 21 2 150 LGYSTDPIRVAKFNWMQCEH 8 7 5 22 5 3 12 3 3 38 1 150 YDSGLARTCEQVNPFHIKWM 9 1 2 12 3 1 26 7 2 4 7 2 150NGYDSWHLPRKETVCIMAFQ 10 19 1 2 2 17 24 5 2 5 1 150 YGAFWHLPTNSVDEIQRCM11 1 1 105 2 2 1 13 14 150 FMLYGIVAEKPQRSWX 12 130 3 5 1 150 DGYEQNHT 131 2 5 5 14 18 1 150 YVLIPSFHTDAMN 80 21 243 38 158 259 46 46 27 127 31 NP Q R S T V W Y | X # 1 2 5 4 8 9 11 8 1 150 GDTESHRVLPAQFIKCNW 2 1 13 320 17 7 5 3 4 150 GRSPALTKVCDYHMQWFEIN 3 3 8 11 8 16 11 7 2 12 150GSYHQTDPRAVLEFKNCMWI 4 1 6 4 4 18 10 6 16 14 1 150 GSWYTIADFLPVEQRCHMNX5 3 6 4 5 19 8 3 7 15 150 GLSYDATWPREQMNVFIH 6 3 15 8 6 16 13 8 3 17 150GYSPTDAQVFRLNWCIKEM 7 4 7 2 6 15 14 6 4 19 150 LGYSTDPIRVAKFNWMQCEH 8 44 5 7 15 7 5 2 29 150 YDSGLARTCEQVNPFHIKWM 9 31 5 1 5 10 3 3 9 16 150NGYDSWHLPRKETVCIMAFQ 10 3 5 2 2 3 4 3 15 35 150 YGAFWHLPTNSVDEIQRCM 11 11 1 1 2 1 3 1 150 FMLYGIVAEKPQRSWX 12 2 3 1 5 150 DGYEQNHT 13 1 14 13 421 51 150 YVLIPSFHTDAMN 58 89 48 72 152 93 77 63 220 2 1950Tally of sequences of length 14 # = 118 A C D E F G H I K L M # 1 6 29 72 32 8 1 1 2 118 GDVHERTAFLPSIKNQ 2 4 10 1 5 22 7 3 4 7 118GPDRYSVHLFAKIQTENW 3 11 2 7 2 3 25 5 1 9 2 118 GVARYLSDITFWCEMPK 4 5 2 77 3 12 4 4 3 6 118 SGVYPDELRTANHIFKWC 5 6 5 12 2 18 2 2 2 4 1 118GYSDTVARCLPFHIKNWMQ 6 6 10 5 4 16 5 3 2 1 118 YGSTDRAEIFVKWLPQMN 7 4 4 14 32 2 2 2 1 118 GSVTYNADFHIKPQRWEM 8 6 1 5 1 4 18 2 5 3 2 118GSYTWAPRDIFNVLHMCE 9 5 2 4 1 2 11 2 1 5 9 1 118 YSGTLVAKNRDWCFHPEIM 10 25 9 2 3 21 2 2 4 118 YGSDNTCQLRFWAEIKPV 11 12 1 3 5 25 2 2 1 118YGWAPVFNEHLTDMQR 12 1 64 5 1 5 12 16 118 FMLGIPSVAHQTY 13 3 97 4 5 1 1 11 118 DGEANQHIKLV 14 2 3 4 12 6 118 YVPILHFANS 73 73 17 195 34 104 24235 48 24 67 25 N P Q R S T V W Y | X # 1 1 2 1 7 2 7 10 118GDVHERTAFLPSIKNQ 2 1 13 2 10 8 2 8 1 10 118 GPDRYSVHLFAKIQTENW 3 2 11 84 13 3 10 118 GVARYLSDITFWCEMPK 4 5 8 6 13 6 12 3 12 118SGVYPDELRTANHIFKWC 5 2 3 1 6 15 10 7 2 18 118 GYSDTVARCLPFHIKNWMQ 6 1 22 7 16 12 4 3 19 118 YGSTDRAEIFVKWLPQMN 7 5 2 2 2 18 12 13 2 10 118GSVTYNADFHIKPQRWEM 8 4 6 6 16 12 4 9 14 118 GSYTWAPRDIFNVLHMCE 9 5 2 514 10 8 4 27 118 YSGTLVAKNRDWCFHPEIM 10 6 2 5 4 13 6 2 3 27 118YGSDNTCQLRFWAEIKPV 11 4 7 1 1 2 6 14 32 118 YGWAPVFNEHLTDMQR 12 4 1 4 13 1 118 FMLGIPSVAHQTY 13 2 2 1 118 DGEANQHIKLV 14 2 14 2 20 53 118YVPILHFANS 38 67 17 65 129 84 111 44 233 1652Tally of sequences of length 15 # = 125 A C D E F G H I K L M # 1 7 26 83 29 1 3 10 125 GDLREASTVNFIPYH 2 6 2 3 22 3 4 1 9 125 RGPLNSTYAVIQEHWDK3 4 4 5 7 2 19 2 6 2 9 2 125 GRYLSVEPIDTACQWFHKMN 4 7 4 14 6 6 15 2 7 57 4 125 GDYAILVEFRKSTCMNPWHQ 5 6 3 10 2 5 18 4 2 3 2 125GSYVDRWAFTICLNEKMP 6 6 2 7 2 5 10 1 5 7 1 125 SRYGTDLWAPFIVNCEQHM 7 8 414 2 2 22 3 3 1 9 1 125 GSDLAVRPYCTHIWEFNKM 8 6 2 4 22 2 2 3 125GYSVWRATDNPLCIKQ 9 4 3 8 4 20 4 3 1 6 125 YGSDLPTRVAFHQCINKW 10 3 4 5 88 17 1 3 7 125 YGEFNTLSRDVCPAIWH 11 4 2 15 3 3 17 1 1 1 125YGDSNPAWEFRTCQHIKV 12 22 3 2 31 3 1 3 3 125 GYAWPSNCHLMFQRVITX 13 71 1 46 30 125 FMLISQTVGPRY 14 115 2 1 1 1 125 DNEFGHPQ 15 3 5 1 1 20 7 1 125YVILPFSCNGHMQ 83 34 225 43 117 245 23 66 15 86 44 N P Q R S T V W Y | X# 1 4 3 10 7 6 6 2 125 GDLREASTVNFIPYH 2 8 11 4 23 7 7 5 3 7 125RGPLNSTYAVIQEHWDK 3 2 7 3 13 9 5 8 3 13 125 GRYLSVEPIDTACQWFHKMN 4 4 4 16 5 5 7 3 13 125 GDYAILVEFRKSTCMNPWHQ 5 3 2 8 18 5 11 8 15 125GSYVDRWAFTICLNEKMP 6 3 6 2 12 24 9 4 7 12 125 SRYGTDLWAPFIVNCEQHM 7 2 67 21 4 8 3 5 125 GSDLAVRPYCTHIWEFNKM 8 4 4 2 7 19 5 12 10 21 125GYSVWRATDNPLCIKQ 9 3 6 4 5 19 6 5 1 23 125 YGSDLPTRVAFHQCINKW 10 8 4 6 78 5 2 29 125 YGEFNTLSRDVCPAIWH 11 7 5 2 3 14 3 1 4 39 125YGDSNPAWEFRTCQHIKV 12 4 7 2 2 6 1 2 8 24 1 125 GYAWPSNCHLMFQRVITX 13 1 21 4 2 2 1 125 FMLISQTVGPRY 14 3 1 1 125 DNEFGHPQ 15 2 7 1 5 33 39 125YVILPFSCNGHMQ 57 74 24 103 165 66 109 52 243 1 1875Distribution of D-JH with number of cys′s    0  1  2 3 4 1248 53 80 1 1Tally of AAs in the YYCar motif A C D E F G H I K L M # 1 1 1 14 1 1383YFDEH 2 4 1 92 11 4 1383 YFHCLSWDR 3 1379 4 1207 3 2 12 2 2 1383AVTSGNDFILRQX 5 14 1 4 18 17 9 187 4 1 1383 RKTSGHAIVNFLQYPEMI 1221 13835 2 112 30 29 11 187 10 1 N P Q R S T V W Y | X # 1 1366 1383 YFDEH 2 13 2 1265 1383 YFHCLSWDR 3 2 2 1383 CRS 4 4 1 2 17 51 79 1 1383AVTSGNDFILRQX 5 7 2 3 992 55 56 9 3 1 1383 RKTSGHAIVNFLQYPEMI 11 2 4 99777 107 88 2 2634 1 1 6915

TABLE 12P Alignment and tabulation of sequences having 3-22 D segmentsD3:3-22_Phz0 YYYDSSGYYY (SEQ ID NO: 448) = GLG Entry Seq1 L1 Seq2 L2 JHP Score 1 hs3d6hcv GRDYYDSGGYFT 12 GRDYYDSGGYFTVAFDI 17 3 6 1.76D + 13(SEQ ID NO: 334) (SEQ ID NO: 335) 2 hs6d4xb7 DRHNYYDSSGSYS 13DRHNYYDSSGSYSDY 15 4 9 4.40D + 12 (SEQ ID NO: 336) (SEQ ID NO: 337) 3hs6d4xg3 DCPAPAKMYYYGSGICT 17 DCPAPAKMYYYGSGICTFDY 20 4 3 6.55D + 04(SEQ ID NO: 338) (SEQ ID NO: 339) 4 hs83x6f2 AFYDSAD 7 AFYDSADDY 9 4 −42.62D + 05 (SEQ ID NO: 340) (SEQ ID NO: 341) 5 hsa230644 RDYYDSSGPEAG 12RDYYDSSGPEAGFDI 15 3 3 6.87D + 10 (SEQ ID NO: 342) (SEQ ID NO: 343) 6hsa239386 DGTLIDTSAYYYL 13 DGTLIDTSAYYYLY 14 4 6 6.87D + 10(SEQ ID NO: 344) (SEQ ID NO: 345) 7 hsa234232 NSSDSS 6 NSSDSSVLDV 10 6−4 6.55D + 04 (SEQ ID NO: 346) (SEQ ID NO: 347) 8 hsa239378 DQVFDSGGYNHR12 DQVFDSGGYNHRFDS 15 4 3 1.07D + 09 (SEQ ID NO: 348) (SEQ ID NO: 349) 9hsa239367 DLEYYYDSGGHYSP 14 DLEYYYDSGGHYSPFHY 17 4 9 1.10D + 12(SEQ ID NO: 350) (SEQ ID NO: 351) 10 hsa239339 DDSSGY 6 DDSSGYYYIDY 11 4−10 1.72D + 10 (SEQ ID NO: 352) (SEQ ID NO: 353) 11 hsa245311GHYYDSPGQYSYS 13 GHYYDSPGQYSYSEY 15 4 3 1.07D + 09 (SEQ ID NO: 354)(SEQ ID NO: 355) 12 hsa240578 GGFRPPPYDYESSAYRTYR 19GGFRPPPYDYESSAYRTYRLDF 22 4 21 2.75D + 11 (SEQ ID NO: 356)(SEQ ID NO: 357) 13 hsa245359 DSDTRAY 7 DSDTRAYYWYFDL 13 2 −7 1.68D + 07(SEQ ID NO: 358) (SEQ ID NO: 359) 14 hsa245028 GRHYYDSSGYYSTPE 15GRHYYDSSGYYSTPENYFDY 20 4 6 1.80D + 16 (SEQ ID NO: 360) (SEQ ID NO: 361)15 hsa245019 DPSYYYDSSGLPL 13 DPSYYYDSSGLPLHGMDV 18 6 9 4.40D + 12(SEQ ID NO: 362) (SEQ ID NO: 363) 16 hsa244991 TYYYDSSGYLLTR 13TYYYDSSGYLLTRYFQH 17 1 3 4.50D + 15 (SEQ ID NO: 364) (SEQ ID NO: 365) 17hsa244945 NAPHYDSSGYYQT 13 NAPHYDSSGYYQTFDY 16 4 6 7.04D + 13(SEQ ID NO: 366) (SEQ ID NO: 367) 18 hsa244943 GYHSSSYA 8 GYHSSSYADAFDI13 3 −7 6.71D + 07 (SEQ ID NO: 368) (SEQ ID NO: 369) 19 hsa245289PIGYCSGGSC 10 PIGYCSGGSCYSFDY 15 4 −4 2.62D + 05 (SEQ ID NO: 370)(SEQ ID NO: 371) 20 hsa240554 THGTYVTSGYYPKI 14 THGTYVTSGYYPKI 14 4 62.68D + 08 (SEQ ID NO: 372) (SEQ ID NO: 373) 21 hsa279533 GATYYYESSGNYP13 GATYYYESSGNYPDY 15 4 9 7.04D + 13 (SEQ ID NO: 374) (SEQ ID NO: 375)22 hsa389177 AFYHYDSTGYPNRRY 15 AFYHYDSTGYPNRRYYFDY 19 4 6 4.29D + 09(SEQ ID NO: 376) (SEQ ID NO: 377) 23 hsa7321 SYSYYYDSSGYWGG 14SYSYYYDSSGYWGGYFDY 18 4 9 4.50D + 15 (SEQ ID NO: 378) (SEQ ID NO: 379)24 hsaj2772 LSPYYYDSSSYH 12 LSPYYYDSSSYHDAFDI 17 3 6 2.62D + 05(SEQ ID NO: 380) (SEQ ID NO: 381) 25 hsb7g4f08 EEDYYDSSGQAS 12EEDYYDSSGQASYNWFXP 18 5 6 2.75D + 11 (SEQ ID NO: 382) (SEQ ID NO: 383)26 hsb7g3b02 ETNYYDSGGYPG 12 ETNYYDSGGYPGFDF 15 4 6 4.40D + 12(SEQ ID NO: 384) (SEQ ID NO: 385) 27 hsb7g3c12 GDHYYDRSGYRH 12GDHYYDRSGYRHSYYYYAMDV 21 6 6 2.75D + 11 (SEQ ID NO: 386)(SEQ ID NO: 387) 28 hsb8g3b07 DRSSGN 6 DRSSGNYFDGMDV 13 6 −10 6.55D + 04(SEQ ID NO: 388) (SEQ ID NO: 389) 29 hsfog1h GRSRYSGYG 9GRSRYSGYGFYSGMDV 16 6 −4 2.62D + 05 (SEQ ID NO: 390) (SEQ ID NO: 391) 30hsgvh0209 DDTSGYGP 8 DDTSGYGPYYFYYGMDV 17 6 −10 2.68D + 08(SEQ ID NO: 392) (SEQ ID NO: 393) 31 hsgvh55 RAYYDTSFYFEY 12RAYYDTSFYFEYY 13 4 3 1.72D + 10 (SEQ ID NO: 394) (SEQ ID NO: 395) 32hsgvh0304 DRIDYYKSGYYLGSA 15 DRIDYYKSGYYLGSADS 17 4 6 1.68D + 07(SEQ ID NO: 396) (SEQ ID NO: 397) 33 hsgvh0332 DTDSSSHYG 9 DTDSSSHYGRFDP13 5 −7 1.68D + 07 (SEQ ID NO: 398) (SEQ ID NO: 399) 34 hsgvh0328VSISHYDSSGRPQRVF 16 VSISHYDSSGRPQRVFYGMDV 21 6 9 1.07D + 09(SEQ ID NO: 400) (SEQ ID NO: 401) 35 hsgvh536 QARENVFYDSSGPTAP 16QARENVFYDSSGPTAPFDH 19 4 15 1.72D + 10 (SEQ ID NO: 402) (SEQ ID NO: 403)36 hshcmg42 VPAGNYYDTSGPDN 14 VPAGNYYDTSGPDNAD 16 4 12 1.72D + 10(SEQ ID NO: 404) (SEQ ID NO: 405) 37 hsig001vh WYYFDTSGYYPRNFYYMDV 19WYYFDTSGYYPRNFYYMDV 19 4 3 2.81D + 14 (SEQ ID NO: 406) (SEQ ID NO: 407)38 hsig13g10 GYYYDSGGNYNG 12 GYYYDSGGNYNGDY 14 4 3 1.10D + 12(SEQ ID NO: 408) (SEQ ID NO: 409) 39 hsighpat3 DLRSYDPSGYYN 12DLRSYDPSGYYNDGFDI 17 3 6 2.75D + 11 (SEQ ID NO: 410) (SEQ ID NO: 411) 40hsigh13g7 GYYYDRGGNCNG 12 GYYYDRGGNCNGDY 14 4 3 6.87D + 10(SEQ ID NO: 412) (SEQ ID NO: 413) 41 hsigh13g1 GYYYDRGGNYNG 12GYYYDRGGNYNGDY 14 4 3 1.10D + 12 (SEQ ID NO: 414) (SEQ ID NO: 415) 42hsighxx20 THYDSSGL 8 THYDSSGLDAFDI 13 3 −4 1.72D + 10 (SEQ ID NO: 416)(SEQ ID NO: 417) 43 hsihr9 DDSSGS 6 DDSSGSYYFDY 11 4 −10 1.07D + 09(SEQ ID NO: 418) (SEQ ID NO: 419) 44 hsihv11 LSGGYYS 7 LSGGYYSDFDY 11 4−13 2.68D + 08 (SEQ ID NO: 420) (SEQ ID NO: 421) 45 hs ej1f GDYSDSSDSYI11 GDYSDSSDSYIDAFDV 16 3 3 1.10D + 12 (SEQ ID NO: 422) (SEQ ID NO: 423)46 hsmvh51 GETYYYDSRGYA 12 GETYYYDSRGYAFDH 15 4 6 2.62D + 05(SEQ ID NO: 424) (SEQ ID NO: 425) 47 hsmvh517 PTRDSSGY 8 PTRDSSGYYVGY 124 −4 1.07D + 09 (SEQ ID NO: 426) (SEQ ID NO: 427) 48 hsmvh0406GSFYYDSSGYPP 12 GSFYYDSSGYPPFDC 15 4 6 6.87D + 10 (SEQ ID NO: 428)(SEQ ID NO: 429) 49 hst14x14 GPYYYDSSGYYL 12 GPYYYDSSGYYLLDY 15 4 61.80D + 16 (SEQ ID NO: 430) (SEQ ID NO: 431) 50 hsvhig2 EEGYYDSSGYYSLGA15 EEGYYDSSGYYSLGASDY 18 4 6 4.50D + 15 (SEQ ID NO: 432)(SEQ ID NO: 433) 51 hsvhia2 RPDSSGSRW 9 RPDSSGSRWYFDY 13 4 −7 6.71D + 07(SEQ ID NO: 434) (SEQ ID NO: 435) 52 hsy14936 GYYDISGYYF 10GYYDISGYYFDAFNI 15 3 −4 2.81D + 14 (SEQ ID NO: 436) (SEQ ID NO: 437) 53hsy14934 DRGYDSSGYYGN 12 DRGYDSSGYYGNLDC 15 4 3 1.76D + 13(SEQ ID NO: 438) (SEQ ID NO: 439) 54 hsy14935 DRGYDSIGYYGN 12DRGYDSIGYYGNLDC 15 4 3 1.10D + 12 (SEQ ID NO: 440) (SEQ ID NO: 441) 55hsz80519 AEDLTYYYDRSGWGVHGLL 19 AEDLTYYYDRSGWGVHGLLYYFDY 24 4 15 4.40D +12 (SEQ ID NO: 442) (SEQ ID NO: 443) 56 hsz80429 LYPHYDSSGYYYV 13LYPHYDSSGYYYVLDY 16 4 6 4.50D + 15 (SEQ ID NO: 444) (SEQ ID NO: 445) 57hsz80461 DRVGYYDSSGYPPGSP 16 DRVGYYDSSGYPPGSPLDY 19 4 9 1.76D + 13(SEQ ID NO: 446) (SEQ ID NO: 447)Frequency of each AA type at each position in 57 Sequences having D3-22 segmentsPos A C D E F G H I K L M N P Q R S T V W Y | X # 1 1 1 2 1 1 3 1 1 1 34 1 1 1 1 4 5 5 1 1 2 1 1 1 12 6 3 3 4 6 3 1 2 2 2 1 1 28 x 7 1 5 4 1 72 1 1 1 3 5 3 4 1 1 1 41 x 8 2 1 4 1 5 3 1 4 4 1 3 1 3 1 14 48 x 9 4 2 35 1 1 1 2 2 2 1 28 52 Y 10 1 4 2 1 1 1 1 4 1 40 56 Y 11 46 2 1 1 1 2 1 357 D 12 1 1 1 1 1 1 4 39 7 1 57 S 13 1 8 1 1 1 1 43 1 57 S 14 3 2 1 45 11 3 56 G 15 2 2 2 5 3 2 1 4 1 33 55 Y 16 2 1 1 1 2 3 1 1 1 6 3 1 1 1 2449 x 17 3 1 1 1 5 2 1 4 6 6 2 7 2 1 1 3 46 x 18 8 1 1 2 2 2 4 3 1 3 2719 2 1 1 1 3 4 1 13 20 2 1 2 1 1 1 1 9 21 1 1 1 3 22 1 1 2 23 1 1 2 24 11 25 1 1 Average Dseg = 11.9 Average DJ = 15.7 Median D = 12 12 Shortest6 Longest 19 Median DJ = 15 15 Shortest 9 Longest 24

TABLE 13P Frequency of D-segments. “|” stands for a stop codon. D seg“0” % C % GLG “1” % C % GLG “2” % C % GLG 1-01 1 0.13 0 VQLERX(SEQ ID 40.53 0.22 GTTGTX(SEQ ID 5 0.66 0.34 YNWND(SEQ ID NO: 132) NO: 133)NO: 134) 1-07 0 0 0 V|LELX(SEQ ID 3 0.4 0.11 GITGTX(SEQ ID 9 1.19 0.34YNWNY(SEQ ID NO: 135) NO: 136) NO: 137) 1-20 0 0 0 V|LERX(SEQ ID 1 0.130.22 GITGTX(SEQ ID 4 0.53 0.45 YNWND(SEQ ID NO: 138) NO: 139) NO: 140)1-26 4 0.53 0 V|WELLX(SEQ ID 13 1.72 0.90 GIVGATX(SEQ ID 36 4.76 0.78YSGSYY(SEQ ID NO: 141) NO: 142) NO: 143) 2-02 31 4.1 2.47 GYCSSTSCYT(SEQ4 0.53 0.22 RIL||YQLLYX(SEQ 9 1.19 2.47 DIVVVPAAIX(SEQ ID NO: 144)ID NO: 145) ID NO: 146) 2-08 5 0.66 0.56 GYCTNGVCYT(SEQ 0 0 0RILY|WCMLYX(SEQ 3 0.4 0.56 DIVLMVYAIX(SEQ ID NO: 147) ID NO: 148)ID NO: 149) 2-15 29 3.83 1.57 GYCSGGSCYS(SEQ 2 0.26 0.11 RIL|WW|LLLX(SEQ7 0.92 1.57 DIVVVVAATX(SEQ ID NO: 150) ID NO: 151) ID NO: 152) 2-21 162.11 0.67 AYCGGDCYS(SEQ 0 0 0 SILWW|LLFX(SEQ 7 0.92 0.67 HIVVVTAIX(SEQID NO: 153) ID NO: 154) ID NO: 155) 3-03 32 4.23 2.80 YYDFWSGYYT(SEQ 70.92 0.90 VLRFLEWLLYX(SEQ 27 3.57 1.12 ITIFGVVIIX(SEQ ID NO: 156)ID NO: 157) ID NO: 158) 3-09 13 1.72 1.35 YYDILTGYYN(SEQ 5 0.66 0.78VLRYFDWLL|X(SEQ 0 0 0 ITIF|LVIIX(SEQ ID NO: 159) ID NO: 160) ID NO: 161)3-10 42 5.55 4.26 YYYGSGSYYN(SEQ 13 1.72 0.89 VLLWFGELL|X(SEQ 11 1.452.91 ITMVRGVIIX(SEQ ID NO: 162) ID NO: 163) ID NO: 164) 3-16 18 2.380.67 YYDYVWGSYRYT 8 1.06 0 VL|LRLGELSLYX 5 0.66 0.34 IMITFGGVIVIX(SEQ ID (SEQ ID NO: 166) (SEQ ID NO: 165) NO: 167) 3-22 57 7.53 3.36YYYDSSGYYY(SEQ 1 0.13 0.11 VLL|||WLLLX 6 0.79 0.34 ITMIVVVITX(SEQID NO: 168) (SEQ ID ID NO: 170) NO: 169) 4-04 5 0.66 0.28 DYSNY(SEQ ID 20.26 0 |LQ|LX(SEQ ID 2 0.26 0.06 TTVTX(SEQ ID NO: 171) NO: 172) NO: 173)4-17 29 3.83 1.45 DYGDY(SEQ ID 0 0 0 |LR|LX(SEQ ID 20 2.64 0.90TTVTX(SEQ ID NO: 174) NO: 175) NO: 176) 4-23 10 1.32 0.56 DYGGNS(SEQ ID1 0.13 0 |LRW|LX(SEQ ID 4 0.53 0.56 TTVVTX(SEQ ID NO: 177) NO: 178)NO: 179) 5-05 3 0.4 0.06 WIQLWLX(SEQ ID 10 1.32 0.39 VDTAMVX(SEQ ID 314.1 0.73 GYSYGY(SEQ ID NO: 180) NO: 181) NO: 182) 5-12 0 0 0WI|WLRLX(SEQ 8 1.06 0.45 VDIVATIX(SEQ 14 1.85 1.12 GYSGYDY(SEQ IDID NO: 183) ID NO: 184) NO: 185) 5-24 11 1.45 0 |RWLQLX(SEQ ID 5 0.660.34 VEMATIX(SEQ ID 13 1.72 0.44 RDGYNY(SEQ ID NO: 186) NO: 187)NO: 188) 6-06 11 1.45 0.78 SIAARX(SEQ ID 9 1.19 0.48 EYSSSS(SEQ ID 10.13 0.11 V|QLVX(SEQ ID NO: 189) NO: 190) NO: 191) 6-13 19 2.51 1.01GIAVAGX(SEQ ID 35 4.62 2.13 GYSSSWY(SEQ ID 2 0.26 0.31 V|QQLVX(SEQ IDNO: 192) NO: 193) NO: 194) 6-19 14 1.85 2.12 GIAVAGX(SEQ ID 48 6.34 2.02GYSSGWY(SEQ ID 4 0.53 0.56 V|QWLVX(SEQ ID NO: 195) NO: 196) NO: 197)D7:7- 1 0.13 0 |LGX 2 0.26 0.68 LTGX(SEQ ID 2 0.26 0.22 NWG 27 NO: 198)Total = 757

TABLE 14P Possible library components. Component L f D2_2-02_Phz0xxxYCSSTSCxxx 13, 31,   (SEQ ID NO: 199) D3_3-16_Phz0 xxxxYVWGSYxxx 13,18,   (SEQ ID NO: 200) D5_5-12_Phz2 xxxxxxxSGYxxx 13, 14,  (SEQ ID NO: 201) D3_3-09_Phz0 xxxYDILTGYYxx 13, 13,   (SEQ ID NO: 202)D2_2-02_Phz2 xxxVVVPAAxxxx 13,  9,   (SEQ ID NO: 203) D3_3-22_Phz0 xxxYYDSSGYxx 12, 57,   (SEQ ID NO: 204) D3_3-03_Phz0  xxxDFWSGxxxx 12,32,   (SEQ ID NO: 205) D3_3-03_Phz2  xxxTIFGVxxxx 12, 27,  (SEQ ID NO: 206) D5_5-12_Phz1  xxxxIVATxxxx 12,  8,   (SEQ ID NO: 207)D3_3-10_Phz0   xxxYGSGSYYx 11, 42, !could add one x at either end (SEQ ID NO:208) D5_5-05_Phz2   xxxxYSYGxxx11, 31,   (SEQ ID NO: 209) D2_2-15_Phz0   xxxCSGxxCYx 11, 29,  (SEQ ID NO: 210) D6_6-13_Phz0   xxxxAAAGxxx 11, 19,   (SEQ ID NO: 211)D4_4-23_Phz0   xGxxxGGNxxx 11, 10,   (SEQ ID NO: 212) D1_1-26_Phz2   xxxSGSYxxx 10, 35,   (SEQ ID NO: 213) D6_6-13_Phz1    xxxSSSWxxx 10,35,   (SEQ ID NO: 214) D4_4-17_Phz2    xxxxTTVTTx 10, 20,  (SEQ ID NO: 215) D2_2-21_Phz0 xxxC(SG)GDxCx 10, 16,   (SEQ ID NO: 216)D6_6-19_Phz0 xxx(IV)AVAGxx 10, 14,   (SEQ ID NO: 217) D3_3-10_Phz1   xxLWFGELxx 10, 13,   (SEQ ID NO: 218) D5_5-24_Phz0    GxxWLxxxxF 10,11,   (SEQ ID NO: 219) D5_5-05_Phz1    xxxDTxMVxx 10, 10,  (SEQ ID NO: 220) D3_3-16_Phz1    xxxxxGExxx 10,  8,   (SEQ ID NO: 221)D6_6-19_Phz1     xxxxSGWxx  9, 48,   (SEQ ID NO: 222) D5_5-24_Phz2    xxxxGYNxx  9, 13,   (SEQ ID NO: 223) D3_3-10_Phz2     xxxVRGVxx  9,11,   (SEQ ID NO: 224) D6_6-06_Phz0     xxxIAAxxx  9, 11,  (SEQ ID NO: 225) D1_1-07_Phz2     xxYxWNxxx  9,  9,   (SEQ ID NO: 226)D4_4-17_Phz0      xxxYGDxx  8, 29,   (SEQ ID NO: 227) D1_1-26_Phz1     xxVGATxx  8, 13,   (SEQ ID NO: 228) D6_6-06_Phz1      xxxYSSSx  8, 9,   (SEQ ID NO: 229)

TABLE 15P Lengths of CDRs: 1095 actual VH domains and 51 VH GLGs. Length0 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 CDR1 0 0 10 0 1 820 38 175 11 5 1 11 0 23 1 7 0 GLG 0 0 0 0 0 38 3 10 0 0 . . . CDR2 0 0 0 0 0 2 0 00 0 0 0 0 0 0 0 464 579 GLG 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 1 17 28 CDR3 00 0 4 2 8 6 28 40 65  77  90 117 117 88 105 86 81 Length 18 19 20 21 2223 24 25 26 27 28 29 30 31 32 (33 or more) CDR2 9 31 1  3  3 1 0 0 0 0 20 0 . . . GLG 1 4 0 0 . . . CDR3 45 36 36 16 16 8 8 2 3 0 2 1 0 0 1 5

TABLE 16P Library of HC CDR3 Component Fraction of Length #X Complexitylibrary Adjusted 1:            YYCA21111YFDYWG. 8 4 2.6 E 5 .10 (0-8).02           (2 = KR; SEQ ID NO: 6) 2:          YYCA2111111YFDYWG. 10 69.4 E 7 .14 (9-10) .14           (2 = KR; SEQ ID NO: 7) 3:       YYCA211111111YFDYTG. 12 8 3.4 E 10 .25 (11 + 12 + 13/2) .25          (2 = KR; SEQ ID NO: 8) 4:      YYCAR111S2S3111YFDYWG. 14 61.9 e 8 .13 (14 + 13/2) .14           (2 = SG 3 = YW; SEQ ID NO: 9) 5:    YYCA2111CSG11CY1YFDYWG. 15 6 9.4 E 7 .13 (15 + 16/2) .14          (2 = KR; SEQ ID NO: 10) 6:   YYCA211S1TIFG11111YFDYWG. 17 81.7 E 10 .11 (17 + 16/2) .12           (2 = KR; SEQ ID NO: 11) 7: YYCAR111YY2S33YY111YFDYWG. 18 6 3.8 E 8 .04 (18) .08     (2 = D|G; 3 =S|G; SEQ ID NO: 12) 8: YYCAR1111YC2231CY111YFDYWG. 19 8 2.0 E 11.10 (19 on) .11     (2 = S G; 3 = T D G; SEQ ID NO: 13) Allowed lengths:8, 10, 12, 14, 15, 17, 18, & 19

TABLE 17P vgDNA encoding the CDR3 elements of the library !CDR3 library components (Ctop25) 5′-gctctggtcaa C|TTA|AGg|gct|gag|g-3′(SEQ ID NO:40) (CtprmA) 5′-gctctggtcaa C|TTA|AGg|gct|gag|gac- !                      AflII . . . |acc|gct|gtc|tac|tac|tgc|gcc-3′(SEQ ID NO: 41) (CBprmB)[RC]5′-|tac|ttc|gat|tac|ttg|ggc|caa|GGT|ACC|ctG|GTC|ACC|tcgctccacc-3′(SEQ ID NO: 42)!                                                      BstEII . . .(CBot25)[RC]                            5′-|GGT|ACC|ctG|GTC|ACC|tcgctccacc-3′(SEQ ID NO: 43)! ! N.B. [RC]means the the actual oligonucleotide is the reverse complement !     of the one shown. ! N.B. The 20 bases at 3′end of CtprmA are identical to the most 5′ 20 bases !     of each of the vgDNA molecules. !N.B. Ctop25 is identical to the most 5′ 25 bases of CtprmA. !N.B. The 23 most 3′ bases of CBprmB are the reverse complement of the !     most 3′ 23 bases of each of the vgDNA molecules. !N.B. CBot25 is identical to the 25 bases at the 5′ end of CBprmB. !(C1t08) 5′-cc|gct|gtc|tac|tac|tgc|gcc|-        <2>|<1>|<1>|<1>|<1>-     |tac|ttc|gat|tac|ttg|ggc|caa|GG-3′ (SEQ ID NO: 44) ! 2 = KR, 1 =0.27Y + 0.27G + 0.027 {ADEFHIKLMNPQRSTVW} no C ! (C2t10)5′-cc|gct|gtc|tac|tac|tgc|gcc|-        <2>|<1>|<1>|<1>|<1>|<1>|<1>|-     tac|ttc|gat|tac|ttg|ggc|caa|GG-3′ (SEQ ID NO: 45) ! 2 = KR, 1 =0.27Y + 0.27G + 0.027 {ADEFHIKLMNPQRSTVW} no C ! (C3t12)5′-cc|gct|gtc|tac|tac|tgc|gcc|-       <2>|<1>|<1>|<1>|<1>|<1>|<1>|<1>|<1>|-     tac|ttc|gat|tac|ttg|ggc|caa|GG-3′ (SEQ ID NO: 46) ! 2 = KR, 1 =0.27Y + 0.27G + 0.027 {ADEFHIKLMNPQRSTVW} no C ! (C4t14)5′-cc|gct|gtc|tac|tac|tgc|gcc|cgt|-     |<1>|<1>|<1>|tct|<2>|tct|<3>|<1>|<1>|<1>|-   tac|ttc|gat|tac|ttg|ggc|caa|GG-3′ (SEQ ID NO: 47) ! 2 = SG, 1 =0.27Y + 0.27G + 0.027 {ADEFHIKLMNPQRSTVW} no C, 3 = YW ! (C5t15)5′-cc|gct|gtc|tac|tac|tgc|gcc|-        <2>|<1>|<1>|<1>|tgc|tct|ggt|<1>|<1>|tgc|tat|<1>|-     tac|ttc|gat|tac|ttg|ggc|caa|GG-3′ (SEQ ID NO: 48) ! 2 = KR, 1 =0.27Y + 0.27G + 0.027 {ADEFHIKLMNPQRSTVW} no C ! (C6t17)5′-cc|gct|gtc|tac|tac|tgc|gcc|-      <2>|<1>|<1>|tct|<1>|act|atc|ttc|ggt|<1>|<1>|<1>|<1>|<1>|-     tac|ttc|gat|tac|ttg|ggc|caa|GG-3′ (SEQ ID NO: 49) ! 2 = KR, 1 =0.27Y + 0.27G + 0.027 {ADEFHIKLMNPQRSTVW} no C ! (C7t18)5′-cc|gct|gtc|tac|tac|tgc|gcc|cgt|-      |<1>|<1>|<1>|tat|tac|<2>|tct|<3>|<3>|tac|tat|<1>|<1>|<1>|-     tac|ttc|gat|tac|ttg|ggc|caa|GG-3′ (SEQ ID NO: 50) ! 2 = DG, 1 =0.27Y + 0.27G + 0.027 {ADEFHIKLMNPQRSTVW} no C, 3 = SG ! (c8t19)5′-cc|gct|gtc|tac|tac|tgc|gcc|cgt|-      |<1>|<1>|<1>|<1>|tat|tgc|<2>|<2>|<3>|<1>|tgc|tat|<1>|<1>|<1>|-     tac|ttc|gat|tac|ttg|ggc|caa|GG-3′ (SEQ ID NO: 51) ! 2 = SG, 1 =0.27Y + 0.27G + 0.027 {ADEFHIKLMNPQRSTVW} no C, 3 = TDG !-----------------------------------------------------------------------------

TABLE 19 Names of 1398 GeneBank entries examined haj10335 hsa006165hsa234190 hsa234288 hsa239366 hsa240594 hsa244963 hs201e3 hsa006167hsa234191 hsa234290 hsa239367 hsa240595 hsa244965 hs201g1 hsa006169hsa234193 hsa234291 hsa239368 hsa240599 hsa244966 hs201m2 hsa006171hsa234194 hsa234294 hsa239369 hsa240604 hsa244967 hs202e2 hsa006173hsa234196 hsa234296 hsa239370 hsa241344 hsa244968 hs202g3 hsa131921hsa234197 hsa234298 hsa239371 hsa241345 hsa244969 hs202g9 hsa132847hsa234199 hsa235649 hsa239372 hsa241346 hsa244970 hs202m3 hsa132849hsa234202 hsa235658 hsa239373 hsa241347 hsa244971 hs203e1 hsa132850hsa234203 hsa235662 hsa239375 hsa241348 hsa244972 hs203g1 hsa132851hsa234205 hsa235664 hsa239376 hsa241349 hsa244973 hs203m5 hsa132852hsa234206 hsa235665 hsa239377 hsa241350 hsa244974 hs204e1 hsa224746hsa234207 hsa235667 hsa239378 hsa241351 hsa244975 hs204g1 hsa225092hsa234208 hsa235671 hsa239379 hsa241353 hsa244976 hs3d6hcv hsa225093hsa234209 hsa235675 hsa239380 hsa241354 hsa244977 hs6d4xa7 hsa230634hsa234211 hsa235677 hsa239381 hsa241355 hsa244978 hs6d4xb7 hsa230635hsa234212 hsa238036 hsa239382 hsa241356 hsa244979 hs6d4xf1 hsa230636hsa234214 hsa238037 hsa239383 hsa241357 hsa244980 hs6d4xf2 hsa230637hsa234217 hsa238038 hsa239384 hsa241420 hsa244981 hs6d4xg3 hsa230638hsa234221 hsa238039 hsa239385 hsa241421 hsa244982 hs6d4xh5 hsa230639hsa234224 hsa238040 hsa239386 hsa242555 hsa244983 hs83x6b2 hsa230640hsa234227 hsa238326 hsa239387 hsa242556 hsa244984 hs83x6b5 hsa230641hsa234229 hsa238327 hsa239388 hsa243108 hsa244985 hs83x6c3 hsa230643hsa234230 hsa238328 hsa239390 hsa243110 hsa244986 hs83x6c4 hsa230644hsa234232 hsa239330 hsa239391 hsa244928 hsa244987 hs83x6c5 hsa230645hsa234235 hsa239331 hsa240553 hsa244929 hsa244988 hs83x6d4 hsa230646hsa234238 hsa239332 hsa240554 hsa244930 hsa244989 hs83x6f1 hsa230647hsa234239 hsa239333 hsa240555 hsa244931 hsa244990 hs83x6f2 hsa230648hsa234242 hsa239334 hsa240556 hsa244932 hsa244991 hs83x6f3 hsa230649hsa234245 hsa239335 hsa240557 hsa244933 hsa244992 hs83x6f5 hsa230650hsa234248 hsa239336 hsa240558 hsa244934 hsa244993 hs83x6h3 hsa230651hsa234249 hsa239337 hsa240559 hsa244935 hsa244994 hs83x9a6 hsa230652hsa234251 hsa239338 hsa240560 hsa244936 hsa244995 hs83x9b6 hsa230653hsa234252 hsa239339 hsa240561 hsa244937 hsa244996 hs83x9b9 hsa230654hsa234255 hsa239340 hsa240562 hsa244938 hsa244997 hs83x9c8 hsa230655hsa234256 hsa239341 hsa240563 hsa244939 hsa244998 hs83x9d6 hsa230656hsa234257 hsa239342 hsa240564 hsa244940 hsa244999 hs83x9d7 hsa230657hsa234258 hsa239343 hsa240565 hsa244941 hsa245000 hs83x9e6 hsa230658hsa234259 hsa239344 hsa240566 hsa244942 hsa245001 hs83x9e8 hsa234156hsa234260 hsa239345 hsa240567 hsa244943 hsa245002 hs83x9e9 hsa234158hsa234262 hsa239346 hsa240568 hsa244944 hsa245003 hs83x9f6 hsa234160hsa234263 hsa239347 hsa240569 hsa244945 hsa245004 hs83x9g6 hsa234161hsa234264 hsa239348 hsa240570 hsa244946 hsa245005 hs9d4x10 hsa234163hsa234266 hsa239349 hsa240571 hsa244947 hsa245006 hs9d4x7 hsa234164hsa234268 hsa239350 hsa240572 hsa244948 hsa245007 hs9d4x8 hsa234166hsa234269 hsa239351 hsa240573 hsa244949 hsa245008 hs9d4x9 hsa234168hsa234270 hsa239353 hsa240575 hsa244950 hsa245009 hs9d4xa6 hsa234169hsa234272 hsa239354 hsa240576 hsa244951 hsa245010 hs9d4xa7 hsa234171hsa234273 hsa239355 hsa240578 hsa244952 hsa245011 hs9d4xb6 hsa234172hsa234274 hsa239356 hsa240580 hsa244953 hsa245012 hs9d4xc2 hsa234175hsa234276 hsa239357 hsa240581 hsa244954 hsa245013 hs9d4xd6 hsa234178hsa234277 hsa239358 hsa240582 hsa244955 hsa245014 hs9d4xe6 hsa234180hsa234279 hsa239359 hsa240585 hsa244956 hsa245015 hs9d4xf3 hsa234181hsa234281 hsa239360 hsa240586 hsa244957 hsa245016 hs9d4xh4 hsa234183hsa234282 hsa239361 hsa240588 hsa244958 hsa245017 hs9d4xh5 hsa234184hsa234283 hsa239362 hsa240589 hsa244959 hsa245018 hsa005975 hsa234186hsa234284 hsa239363 hsa240590 hsa244960 hsa245019 hsa005977 hsa234187hsa234286 hsa239364 hsa240592 hsa244961 hsa245020 hsa006161 hsa234189hsa234287 hsa239365 hsa240593 hsa244962 hsa245021 hsa245022 hsa245217hsa245305 hsa279524 hsabhiv8 hsb8g2g08 hsevh52a1 hsa245023 hsa245218hsa245307 hsa279526 hsadeigvh hsb8g3b07 hsevh52a2 hsa245024 hsa245219hsa245309 hsa279527 hsaj2768 hsb8g3c07 hsevh52a3 hsa245025 hsa245220hsa245311 hsa279528 hsaj2769 hsb8g3c08 hsevh52a4 hsa245026 hsa245221hsa245312 hsa279529 hsaj2771 hsb8g3c12 hsevh52a5 hsa245027 hsa245222hsa245313 hsa279530 hsaj2772 hsb8g3d03 hsevh52b1 hsa245028 hsa245223hsa245315 hsa279531 hsaj2773 hsb8g3d04 hsevh53a1 hsa245029 hsa245224hsa245317 hsa279532 hsaj2776 hsb8g3d07 hsevh53a2 hsa245030 hsa245225hsa245318 hsa279533 hsaj2777 hsb8g3d08 hsfog1h hsa245031 hsa245226hsa245319 hsa279535 hsaj4083 hsb8g3e02 hsfog3h hsa245032 hsa245228hsa245320 hsa279536 hsaj4899 hsb8g3e03 hsfogbh hsa245033 hsa245229hsa245321 hsa279537 hsasighc hsb8g3f03 hsfom1h hsa245034 hsa245230hsa245322 hsa279543 hsavh510 hsb8g3g01 hsfs10hc hsa245035 hsa245231hsa245323 hsa279544 hsavh512 hsb8g3g03 hsfs11hc hsa245036 hsa245232hsa245325 hsa279545 hsavh513 hsb8g3g05 hsfs9whc hsa245037 hsa245233hsa245326 hsa279552 hsavh514 hsb8g3g10 hsgad2h hsa245039 hsa245234hsa245338 hsa389169 hsavh515 hsb8g3h01 hsgvh0117 hsa245040 hsa245235hsa245342 hsa389170 hsavh516 hsb8g4c02 hsgvh0118 hsa245041 hsa245236hsa245343 hsa389171 hsavh517 hsb8g4e01 hsgvh0119 hsa245042 hsa245237hsa245345 hsa389172 hsavh519 hsb8g4e05 hsgvh0120 hsa245043 hsa245238hsa245346 hsa389173 hsavh520 hsb8g4f11 hsgvh0121 hsa245044 hsa245239hsa245347 hsa389174 hsavh523 hsb8g4h09 hsgvh0122 hsa245045 hsa245240hsa245348 hsa389175 hsavh524 hsb8g4h10 hsgvh0123 hsa245046 hsa245241hsa245349 hsa389176 hsavh526 hsb8g5d10 hsgvh0124 hsa245047 hsa245246hsa245350 hsa389177 hsavh529 hsb8g5h08 hsgvh0201 hsa245048 hsa245251hsa245352 hsa389178 hsavh53 hsbel1 hsgvh0202 hsa245049 hsa245255hsa245353 hsa389179 hsavh56 hsbel14 hsgvh0203 hsa245050 hsa245258hsa245355 hsa389180 hsb3g4a07 hsbel28 hsgvh0204 hsa245051 hsa245260hsa245356 hsa389181 hsb73g04n hsbel29 hsgvh0205 hsa245052 hsa245261hsa245357 hsa389182 hsb74a08n hsbel3 hsgvh0206 hsa245053 hsa245262hsa245358 hsa389183 hsb7g1a11 hsbel34 hsgvh0207 hsa245054 hsa245263hsa245359 hsa389184 hsb7g2b01 hsbel43 hsgvh0208 hsa245055 hsa245265hsa249378 hsa389185 hsb7g3a01 hsbel45 hsgvh0209 hsa245056 hsa245266hsa249628 hsa389186 hsb7g3a05 hsbel5 hsgvh0210 hsa245057 hsa245268hsa249629 hsa389187 hsb7g3a10 bsbel54 hsgvh0211 hsa245058 hsa245272hsa249630 hsa389188 hsb7g3b02 bsbel69 hsgvh0213 hsa245059 hsa245273hsa249631 hsa389190 hsb7g3b03 hsbo1vhig hsgvh0214 hsa245060 hsa245275hsa249632 hsa389191 hsb7g3b05 hsbo3vhig hsgvh0215 hsa245061 hsa245277hsa249633 hsa389192 hsb7g3c03 hsbr1vhig hsgvh0216 hsa245062 hsa245278hsa249634 hsa389193 hsb7g3c12 hsbradh3 hsgvh0217 hsa245063 hsa245279hsa249635 hsa389194 hsb7g3d07 hscal4ghc hsgvh0218 hsa245064 hsa245280hsa249636 hsa389195 hsb7g3e01 hsd4xd10 hsgvh0219 hsa245065 hsa245281hsa249637 hsa389927 hsb7g3f02 hsd4xf21 hsgvh0220 hsa245066 hsa245282hsa271600 hsa389929 hsb7g3f10 hsd4xg2 hsgvh0221 hsa245067 hsa245283hsa271601 hsa6351 hsb7g3g02 hsd4xi10 hsgvh0222 hsa245068 hsa245284hsa271602 hsa7321 hsb7g3g04 hsd4xi4 hsgvh0223 hsa245069 hsa245285hsa271603 hsa7322 hsb7g4a08 hsd4xk9 hsgvh0224 hsa245071 hsa245286hsa271604 hsa7323 hsb7g4c05 hsd4xl3 hsgvh0302 hsa245072 hsa245287hsa279513 hsa7325 hsb7g4d09 hsd5hc hsgvh0304 hsa245073 hsa245288hsa279514 hsa7326 hsb7g4f08 hsdo1vhig hsgvh0306 hsa245201 hsa245289hsa279515 hsa7328 hsb7g4g07 hseliepa1 hsgvh0307 hsa245203 hsa245290hsa279516 hsa7438 hsb7g5g03 hseliepa3 hsgvh0308 hsa245204 hsa245291hsa279517 hsa7440 hsb8g1c04 hseliepa4 hsgvh0309 hsa245208 hsa245292hsa279519 hsa7441 hsb8g1e04 hseliepb2 hsgvh0310 hsa245209 hsa245294hsa279520 hsa7442 hsb8g1f03 hseliepd2 hsgvh0311 hsa245210 hsa245298hsa279521 hsa7443 hsb8g1g04 hselilpb1 hsgvh0312 hsa245214 hsa245299hsa279522 hsa7444 hsb8g1h02 hsevh51a1 hsgvh0314 hsa245215 hsa245301hsa279523 hsaarma1 hsb8g2f09 hsevh51b1 hsgvh0315 hsgvh0318 hsig001vhhsighpat5 hsigvhc07 hsimghc1 hsmvh0401 hsrou233 hsgvh0320 hsig030vhhsighpat6 hsigvhc08 hsimghc2 hsmvh0403 hsrt792hc hsgvh0321 hsig033vhhsighpat7 hsigvhc09 hsimghc3 hsmvh0404 hsrt79hc hsgvh0322 hsig039vhhsighpat8 hsigvhc10 hsimghc4 hsmvh0405 hssm1vhig hsgvh0323 hsig040vhhsighpat9 hsigvhc11 hsimghcS hsmvh0406 hssp46a hsgvh0324 hsig055vhhsighpt11 hsigvhc12 hsin42p5 hsmvh0501 hst14vh hsgvh0325 hsig057vhhsighpt12 hsigvhc14 hsin51p7 hsmvh0502 hst14x1 hsgvh0326 hsig1059hsighpta1 hsigvhc16 hsin51p8 hsmvh0503 hst14x10 hsgvh0327 hsig10610hsighvb5 hsigvhc17 hsin78 hsmvh0504 hst14x11 hsgvh0328 hsig13g10hsighvca hsigvhc18 hsin87 hsmvh0505 hst14x12 hsgvh0329 hsig473 hsighvcbhsigvhc19 hsin89p2 hsmvh0506 hst14x13 hsgvh0330 hsig7sa11 hsighvcchsigvhc20 hsin92 hsmvh0507 hst14x14 hsgvh0331 hsigaehc hsighvcdhsigvhc21 hsin98p1 hsmvh0508 hst14x15 hsgvh0332 hsigaf2h2 hsighvcehsigvhc22 hsjac10h hsmvh0509 hst14x16 hsgvh0333 hsigashc hsighvmhsigvhc23 hsjhba1f hsmvh0510 hst14x17 hsgvh0334 hsigathc hsighxx1hsigvhc24 hsjhbr2f hsmvh0511 hst14x18 hsgvh0335 hsigdvrhc hsighxx10hsigvhc25 hsjhej1f hsmvh0513 hst14x19 hsgvh0336 hsigg1kh hsighxx11hsigvhc26 hsld1110 hsmvh0515 hst14x20 hsgvh0419 hsigg1kl hsighxx12hsigvhc27 hsld1117 hsmvh0529 hst14x21 hsgvh0420 hsigg1lh hsighxx14hsigvhc28 hsld152 hsmvh51 hst14x22 hsgvh0421 hsigghc85 hsighxx16hsigvhc29 hsld21 hsmvh510 hst14x23 hsgvh0422 hsigghcv3 hsighxx18hsigvhc30 hsld217 hsmvh511 hst14x24 hsgvh0423 hsigghevr hsighxx2hsigvhc31 hsld218 hsmvh512 hst14x25 hsgvh0424 hsiggvdj1 hsighxx20hsigvhc32 hsld25 hsmvh515 hst14x3 hsgvh0428 hsiggvdj2 hsighxx21hsigvhc33 hsmad2h hsmvh516 hst14x6 hsgvh0429 hsiggvhb hsighxx22hsigvhc35 hsmbcl5h4 hsmvh517 hst14x7 hsgvh0430 hsiggvhc hsighxx23hsigvhc36 hsmica1h hsmvh53 hst14x8 hsgvh0517 hsigh10g1 hsighxx25hsigvhc37 hsmica3h hsmvh54 hst14x9 hsgvh0519 hsigh10g2 hsighxx26hsigvhc38 hsmica4h hsmvh55 hst22x1 hsgvh0522 hsigh10g3 hsighxx28hsigvhc39 hsmica5h hsmvh56 hst22x11 hsgvh0523 hsigh10g4 hsighxx29hsigvhc40 hsmica6h hsmvh57 hst22x12 hsgvh0526 hsigh10g5 hsighxx3hsigvhc41 hsmica7h hsmvh58 hst22x13 hsgvh0527 hsigh10g7 hsighxx30hsigvhc42 hsmt11ige hsmvh59 hst22x14 hsgvh0531 hsigh10g8 hsighxx31hsigvhc43 hsmt12ige hsnamembo hst22x15 hsgvh511 hsigh10g9 hsighxx32hsigvhls hsmt13ige hsnpb346e hst22x18 hsgvh512 hsigh13g1 hsighxx34hsigvhttd hsmt14ige hsoak3h hst22x20 hsgvh513 hsigh13g7 hsighxx36hsigvp151 hsmt15ige hsog31h hst22x21 hsgvh515 hsigh14g1 hsighxx37hsigvp152 hsmt16ige hspag1h hst22x22 hsgvh519 hsigh14g2 hsighxx38hsigvp153 hsmt17ige hsrael hst22x23 hsgvh521 hsigh2f2 hsighxx5 hsigvp154hsmt21ige hsregah hst22x25 hsgvh526 hsigh3135 hsighxx6 hsigvp155hsmt22ige hsrfabh37 hst22x26 hsgvh530 hsigh35 hsighxx7 hsigvp156hsmt23ige hsrighvja hst22x27 hsgvh533 hsigh44 hsighxx8 hsigvp157hsmt24ige hsrighvjb hst22x28 hsgvh534 hsigh4c2 hsighxx9 hsigvp158hsmt25ige hsrou10 hst22x30 hsgvh535 hsigh9e1 hsigkrf hsigvp251 hsmt26igehsrou11 hst22x9 hsgvh536 hsighadi2 hsigmhavh hsigvp255 hsmt27igehsrou111 hsu24687 hsgvh55 hsighadi3 hsigrhe15 hsigvp256 hsmutuiemhsrou112 hsu24688 hsh217e hsighcvr hsigtgk1h hsigvp257 hsmvh0001hsrou119 hsu24690 hsh241e hsighcza hsigtgk4h hsigvp360 hsmvh0002hsrou122 hsu24691 hsh28e hsighczb hsigtgl9h hsigvp363 hsmvh0003 hsrou126hsv52a512 hsha3d1ig hsighczc hsigvarh1 hsigvp369 hsmvh0004 hsrou127hsvdj10h hshambh hsighczd hsigvhc hsigvp39 hsmvh0005 hsrou129 hsvdj12hhshcmg42 hsighczf hsigvhc01 hsihr8 hsmvh0006 hsrou13 hsvgcg1 hshcmg43hsighczg hsigvhc02 hsihr9 hsmvh0007 hsrou131 hsvgcm1 hshcmg44 hsigheavyhsigvhc03 hsihv1 hsmvh0009 hsrou18 hsvgcm2 hshcmg46 hsighpat2 hsigvhc04hsihv11 hsmvh0010 hsrou219 hsvh1djh6 hshcmt42 hsighpat3 hsigvhc05hsihv18 hsmvh0011 hsrou221 hsvh3djh4 hshcmt47 hsighpat4 hsigvhc06hsim9vch hsmvh0012 hsrou222 hsvh4dj hsvh4djh6 hsvhic11 hsww1p10ehsy14935 hsz80377 hsz80424 hsz80482 hsvh4r hsvhic2 hsx98932 hsy14936hsz80378 hsz80426 hsz80483 hsvh52a43 hsvhic3 hsx98933 hsy14937 hsz80383hsz80427 hsz80487 hsvh52a55 hsvhid1 hsx98934 hsy14938 hsz80385 hsz80429hsz80489 hsvh5dj hsvhid5 hsx98935 hsy14939 hsz80386 hsz80433 hsz80492hsvh5djh5 hsvhid7 hsx98936 hsy14940 hsz80388 hsz80436 hsz80495 hsvh710p1hsvhid9 hsx98938 hsy14943 hsz80390 hsz80438 hsz80496 hsvheg7 hsvhie4hsx98939 hsy14945 hsz80391 hsz80439 hsz80499 hsvhfa2 hsvhif10 hsx98940hsy18120 hsz80392 hsz80441 hsz80500 hsvhfa7 hsvhif3 hsx98941 hsz74663hsz80393 hsz80442 hsz80502 hsvhfb5 hsvhif7 hsx98943 hsz74665 hsz80394hsz80443 hsz80504 hsvhfc2 hsvhig2 hsx98944 hsz74668 hsz80397 hsz80445hsz80507 hsvhfd7 hsvhp2 hsx98945 hsz74671 hsz80400 hsz80458 hsz80509hsvhfe5 hsvhp29 hsx98946 hsz74672 hsz80403 hsz80459 hsz80512 hsvhfg9hsvhp30 hsx98947 hsz74682 hsz80406 hsz80460 hsz80513 hsvhgd8 hsvhp32hsx98948 hsz74688 hsz80407 hsz80461 hsz80517 hsvhgd9 hsvhp34 hsx98950hsz74690 hsz80409 hsz80462 hsz80519 hsvhgh7 hsvhp4 hsx98951 hsz74693hsz80411 hsz80463 hsz80520 hsvhha10 hsvhp46 hsx98952 hsz74695 hsz80412hsz80465 hsz80527 hsvhia2 hsvhp48 hsx98953 hsz80363 hsz80414 hsz80466hsz80534 hsvhia5 hsvhp53 hsx98954 hsz80364 hsz80415 hsz80473 hsz80538hsvhib12 hsvhp7 hsx98955 hsz80365 hsz80416 hsz80474 hsz80544 hsvhib6hsvigd9 hsx98956 hsz80367 hsz80417 hsz80475 hsz80545 hsvhib8 hswad35vhhsx98958 hsz80368 hsz80418 hsz80476 hsvhic1 hswanembo hsx98963 hsz80372hsz80421 hsz80477 hsvhic10 hswo1vhig hsy14934 hsz80375 hsz80422 hsz80480

TABLE 20P Human GLG CDR1 & CDR2 AA seqs  CDR1          1    1   1  Name1234567 CDR2 1234567890123456789 1-02 GYY-MH (SEQ ID NO: 230)WINPNSGG--TNYAQKFQG (SEQ ID NO: 231)  1-03 SYA--MH (SEQ ID NO: 232)WINAGNGN--TKYSQKFQG (SEQ ID NO: 233)  1-08 SYD--IN (SEQ ID NO: 234)WMNPNSGN--TGYAQKFQG (SEQ ID NO: 235)  1-18 SYG--IS (SEQ ID NO: 236)WISAYNGN--TNYAQKLQG (SEQ ID NO: 237)  1-24 ELS--MH (SEQ ID NO: 238)GFDPEDGE--TIYAQKFQG (SEQ ID NO: 239)  1-45 YRY--LH (SEQ ID NO: 240)WITPFNGN--TNYAQKFQD (SEQ ID NO: 241)  1-46 SYY--MH (SEQ ID NO: 242)IINPSGGS--TSYAQKFQG (SEQ ID NO: 243)  1-58 SSA--VQ (SEQ ID NO: 244)WIVVGSGN--TNYAQKFQE (SEQ ID NO: 245)  1-69 SYA--IS (SEQ ID NO: 246)GIIPIFGT--ANYAQKFQG (SEQ ID NO: 247)  1-e SYA--IS (SEQ ID NO: 248)GIIPIFGT--ANYAQKFQG (SEQ ID NO: 249)  1-f DYY--MH (SEQ ID NO: 250)LVDPEDGE--TIYAEKFQG (SEQ ID NO: 251)  2-05 TSGVGVG (SEQ ID NO: 252)LIYWNDDK---RYSPSLKS (SEQ ID NO: 253)  2-26 NARMGVS (SEQ ID NO: 254)HIFSNDEK---SYSTSLKS (SEQ ID NO: 255)  2-70 TSGMRVS (SEQ ID NO: 256)RIDWDDDK---FYSTSLKT (SEQ ID NO: 257)  3-07 SYW--MS (SEQ ID NO: 258)NIKQDGSE--KYYVDSVKG (SEQ ID NO: 259)  3-09 DYA--MH (SEQ ID NO: 260)GISWNSGS--IGYADSVKG (SEQ ID NO: 261)  3-11 DYY--MS (SEQ ID NO: 262)YISSSGST--IYYADSVKG (SEQ ID NO: 263)  3-13 SYD--MH (SEQ ID NO: 264)AIGTAGD---TYYPGSVKG (SEQ ID NO: 265)  3-15 NAW--MS (SEQ ID NO: 266)RIKSKTDGGTTDYAAPVKG (SEQ ID NO: 267)  3-20 DYG--MS (SEQ ID NO: 268)GINWNGGS--TGYADSVKG (SEQ ID NO: 269)  3-21 SYS--MN (SEQ ID NO: 270)SISSSSSY--IYYADSVKG (SEQ ID NO: 271)  3-23 SYA--MS (SEQ ID NO: 272)AISGSGGS--TYYADSVKG (SEQ ID NO: 273)  3-30 SYG--MH (SEQ ID NO: 274)VISYDGSN--KYYADSVKG (SEQ ID NO: 275)  3303 SYA--MH (SEQ ID NO: 276)VISYDGSN--KYYADSVKG (SEQ ID NO: 277)  3305 SYG--MH (SEQ ID NO: 278)VISYDGSN--KYYADSVKG (SEQ ID NO: 279)  3-33 SYG--MH (SEQ ID NO: 280)VIWYDGSN--KYYADSVKG (SEQ ID NO: 281)  3-43 DYT--MH (SEQ ID NO: 282)LISWDGGS--TYYADSVKG (SEQ ID NO: 283)  3-48 SYS--MN (SEQ ID NO: 284)YISSSSST--IYYADSVKG (SEQ ID NO: 285)  3-49 DYA--MS (SEQ ID NO: 286)FIRSKAYGGTTEYTASVKG (SEQ ID NO: 287)  3-53 SNY--MS (SEQ ID NO: 288)VIYSGGS---TYYADSVKG (SEQ ID NO: 289)  3-64 SYA--MH (SEQ ID NO: 290)AISSNGGS--TYYANSVKG (SEQ ID NO: 291)  3-66 SNY--MS (SEQ ID NO: 292)VIYSGGS---TYYADSVKG (SEQ ID NO: 293)  3-72 DHY--MD (SEQ ID NO: 294)RTRNKANSYTTEYAASVKG (SEQ ID NO: 295)  3-73 GSA--MH (SEQ ID NO: 296)RIRSKANSYATAYAASVKG (SEQ ID NO: 297)  3-74 SYW--MH (SEQ ID NO: 298)RINSDGSS--TSYADSVKG (SEQ ID NO: 299)  3-d SNE--MS (SEQ ID NO: 300)SISGGS----TYYADSRKG (SEQ ID NO: 301)  4-04 SSNW-WS (SEQ ID NO: 302)EIYHSGS---TNYNPSLKS (SEQ ID NO: 303)  4-28 SSNW-WG (SEQ ID NO: 304)YIYYSGS---TYYNPSLKS (SEQ ID NO: 305)  4301 SGGYYWS (SEQ ID NO: 306)YIYYSGS---TYYNPSLKS (SEQ ID NO: 307)  4302 SGGYSWS (SEQ ID NO: 308)YIYHSGS---TYYNPSLKS (SEQ ID NO: 309)  4304 SGDYYWS (SEQ ID NO: 310)YIYYSGS---TYYNPSLKS (SEQ ID NO: 311)  4-31 SGGYYWS (SEQ ID NO: 312)YIYYSGS---TYYNPSLKS (SEQ ID NO: 313)  4-34 GYY--WS (SEQ ID NO: 314)EINHSGS---TNYNPSLKS (SEQ ID NO: 315)  4-39 SSSYYWG (SEQ ID NO: 316)SIYYSGS---TYYNPSLKS (SEQ ID NO: 317)  4-59 SYY--WS (SEQ ID NO: 318)YIYYSGS---TNYNPSLKS (SEQ ID NO: 319)  4-61 SGSYYWS (SEQ ID NO: 320)YIYYSGS---TNYNPSLKS (SEQ ID NO: 321)  4-b SGYY-WG (SEQ ID NO: 322)SIYHSGS---TYYNPSLKS (SEQ ID NO: 323)  5-51 SYW--IG (SEQ ID NO: 324)IIYPGDSD--TRYSPSFQG (SEQ ID NO: 325)  5-a SYW--IS (SEQ ID NO: 326)RIDPSDSY--TNYSPSFQG (SEQ ID NO: 327)  6-1 SNSAAWN (SEQ ID NO: 328)RTYYRSKWY-NDYAVSVKS (SEQ ID NO: 329)  74.1 SYA--MN (SEQ ID NO: 330)WINTNTGN--PTYAQGFTG (SEQ ID NO: 331)  CDR1 of human GLGs A C D E F G H IK L M N P Q R S T V W Y — Consens. 1 7 1 3 2 35 2 1 Sd x 2 2 6 1 1 4 1 729 Ysg x 3 11 3 1 10 2 1 6 1 5 11 YAGS x 4 1 2 1 2 7 38 — 5 1 2 1 1 5 41— 6 6 1 28 4 12 Mwi 7 1 5 16 5 1 23 SHng CDR2 of human GLGs A C D E F GH I K L M N P Q R S T V W Y — Consens. 1 3 2 1 5 1 2 3 1 7 4 6 7 9 X 2 146 1 2 1 I 3 4 1 1 2 2 8 3 12 1 1 1 15 ysn x 4 2 2 4 1 10 1 11 2 1 5 12ysp x 5 1 8 2 1 6 2 4 8 1 17 1 sd x 6 3 7 2 26 3 8 2 Gsd x 7 4 1 17 1 224 1 1 SG x 8 1 3 3 3 10 9 4 1 2 15 —ns 9 2 3 46 — 10 1 3 47 — 11 2 4 51 1 35 3 T 12 1 2 2 1 3 2 1 11 2 3 1 22 Yn x 13 51 Y 14 31 11 1 6 1 1An x 15 4 16 1 1 1 14 11 2 1 dpq x 16 1 11 1 38 Sk 17 13 15 1 22 Vlf 1837 13 1 Kq 19 1 1 34 14 1 GS

TABLE 21P Tallies of Amino-acid frequencies in mature CDR1 and CDR2Tally of 23 examples with length 14 A C D E F G H I K L M N P Q R S T VW Y | X 1 8 2 13 2 3 15 3 2 3 2 1 14 1 5 4 2 2 11 5 3 5 7 1 1 13 1 6 1 43 12 2 1 7 3 1 1 2 1 5 10 8 6 1 1 2 1 6 4 2 9 1 5 1 3 1 4 7 1 10 1 8 3 12 1 4 1 2 11 1 1 1 1 2 1 16 12 1 2 1 1 1 1 1 1 14 13 4 2 17 14 4 1 5 4 54 Tally of 11 examples with length 12 A C D E F G H I K L M N P Q R S TV W Y | X 1 4 7 2 1 4 4 2 3 7 4 4 1 1 1 5 2 1 5 1 9 1 6 2 1 3 2 3 7 3 13 1 3 8 1 3 2 1 2 2 9 1 1 9 10 1 10 11 11 12 2 1 7 1 Tally of 175examples with length 7 A C D E F G H I K L M N P Q R S T V W Y | X 1 2 11 2 1 3 2 153 10 2 3 2 1 87 1 10 1 5 61 2 2 3 3 26 1 54 1 5 1 2 76 3 1 24 6 1 1 6 1 2 1 11 1 145 5 5 2 13 2 2 3 6 2 140 6 1 1 1 13 159 7 2 1 671 10 88 5 1 Tally of 38 examples with length 6 A C D E F G H I K L M N PQ R S T V W Y | X 1 2 34 2 2 1 2 1 8 4 22 3 3 26 9 4 1 1 29 7 5 38 6 103 22 3 Tally of 820 examples with length 5 A C D E F G H I K L M N P Q RS T V W Y Seen 1 8 81 10 151 4 8 5 3 100 4 15 364 55 8 4 SGNDT x 15 2 75 12 24 1 30 1 1 5 26 1 1 23 2 681 Y 15 3 202 4 24 13 13 133 10 2 7 5 23 32 14 13 112 231 YAGW x 17 4 6 172 2 7 409 3 16 205 MWI 8 5 8 6 1 1 49241 2 79 1 3 367 56 2 4 SHNT x 14 CDR2 Tally of 31 examples with CDR2 oflength 19 A C D E F G H I K L M N P Q R S T V W Y X 1 11 1 1 1 15 1 1 RFx 2 1 28 2 I 3 9 1 18 1 1 1 Rk 4 1 2 6 21 1 S 5 1 1 1 22 1 1 1 1 1 1 K x6 16 1 1 1 1 3 1 6 1 A x 7 1 9 7 3 1 10 y x 8 23 1 1 5 1 G 9 2 18 1 1 17 1 G 10 4 1 1 1 1 1 21 1 T 11 1 3 1 26 T 12 2 11 9 1 1 1 1 2 1 2 x 13 11 29 Y 14 29 1 1 A 15 25 3 1 1 1 A 16 1 10 20 Sp 17 1 1 29 V 18 1 27 1 2K 19 1 30 G Tally of 579 (n > 50, bold; over 400, underscored) exampleswith length 17 A C D E F G H I K L M N P Q R S T V W Y X 1 44 1 1 2 1181 5 69 1 14 6 41 1 4 34 30 19 118 66 31 VGIW x 2 7 522 1 10 17 1 3 8 10I 3 3 1 22 5 7 6 51 25 1 76 8 262 19 1 46 46 SNI x 4 39 2 8 6 16 64 9 32 3 15 178 23 6 50 11 8 16 120 PYG x 5 3 194 6 1 70 6 44 6 4 1 55 4 8133 9 7 1 27 DSGN x 6 3 1 75 4 45 326 1 6 43 1 63 8 1 2 GDS x 7 8 24 5226 3 3 3 4 24 2 11 245 14 6 1 SG x 8 4 2 57 37 5 22 4 18 18 2 2 161 1 411 106 90 2 1 32 NST X 9 56 11 2 63 157 1 3 3 11 5 13 4 242 8 TKIA x 101 14 2 13 30 23 6 29 2 3 110 3 52 20 10 1 1 259 YNR x 11 1 2 7 5 1 4 3 5551 Y 12 405 2 18 1 6 2 3 1 89 8 44 A 13 7 323 22 7 4 1 4 66 138 3 1 3DQP x 14 2 5 6 3 123 1 4 2 7 421 1 2 2 SK x 15 1 1 188 2 1 22 3 1 357 21 VF 16 1 13 1 1 332 3 2 1 1 199 21 4 KQ x 17 11 1 565 1 1 G Tally of464 (over 50, bold; over 400, underscored) A C D E F G H I K L M N P Q RS T V W Y X 1 5 13 184 8 1 7 1 2 15 6 3 26 65 9 14 105 EYSL x 2 6 429 34 1 2 19 I 3 1 13 13 4 10 5 154 1 12 1 250 YN x 4 1 12 2 6 199 2 1 3 4 52 19 28 15 165 YH x 5 5 20 1 1 18 4 9 1 22 365 16 1 1 S x 6 13 8 439 1 11 1 G 7 20 2 14 2 4 2 26 1 12 357 20 1 2 1 S x 8 13 2 4 8 1 2 4 3 6 4201 T 9 10 4 1 10 1 8 1 245 13 9 3 1 1 157 NY x 10 6 2 2 2 1 7 444 Y 11 143 1 1 8 408 4 21 2 2 N 12 4 13 4 2 1 418 14 7 1 P 13 2 2 6 452 1 1 S 142 2 441 1 18 L 15 18 413 3 5 11 10 1 2 1 K 16 1 1 31 2 2 3 419 5 S

TABLE 22P Tally of VH types 1-02 16 1-03 16 1-08 13 1-18 27 1-24 5 1-450 1-46 14 1-58 1 1-69 37 1-e 16 1-f 1 2-05 13 2-26 1 2-70 2 3-07 33 3-0913 3-11 15 3-13 4 3-15 10 3-20 4 3-21 25 3-23 85 3-30 55 3303 59 3305 03-33 42 3-43 1 3-48 24 3-49 11 3-53 12 3-64 4 3-66 4 3-72 3 3-73 3 3-7412 3-d 0 4-04 29 4-28 3 4301 46 4302 7 4304 37 4-31 0 4-34 184 4-39 654-59 45 4-61 9 4-b 11 5-51 55 5-a 13 6-1 7 74.1 3

TABLE 23P Oligonucleotides used to variegate CDR1 and CDR2 of human HC!(name) 5′-....DNA sequence....-3′!everything to right of an exclamation point is commentary ![RC]means “reverse complement” of sequence shown !If last non-comment and non-blank character is “-”, then continue !on next line. ! Ignore case, “a” = “A”, “c” = “C”, etc. ! Ignore “|”and blanks. ! <number>means incorporate trinucleotide mixtue of given number.!-------------------------------------------------------------------------! ! CDR1 (ON-R1V1vg) 5′-       ct|TCC|GGA|ttc|act|ttc|tct|-       <1>|tac|<1>|atg|<1>|-              ! CDR1 of length 5, ON =55 bases                   tgg|gtt|cgC|CAa|gct|ccT|GG-3′ (SEQ ID NO: 27)! <1> = ADEFGHIKLMNPQRSTVWY        no C !(ON-R1top) 5′-cctactgtct |TCC|GGA|ttc|act|ttc|tct-3′ (SEQ ID NO: 28)(ON-R1bot)[RC] 5′-tgg|gtt|cgC|CAa|gct|ccT|GG ttgctcactc-3′(SEQ ID NO: 29) (ON-R1V2vg) 5′-      ct|TCC|GGA|ttc|act|ttc|tct|-       <6>|<7>|<7>|tac|tac|tgg|<7>|-     ! CDR1 of length 7, ON =61 bases                   tgg|gtt|cgC|CAa|gct|ccT|GG-3′ (SEQ ID NO: 30)! <6> = ST, 1:1 ! <7> = 0.2025(SG) + 0.035(ADEFHIKLMNPQRTVWY)   no C(ON-R1V3vg) 5′-ct|TCC|GGA|ttc|act|ttc|tct|-      |atc|agc|ggt|ggt|tct|atc|tcc|<1>|<1>|<1>|tac|tac|tgg|<1>|- !CDR1, L = 14               tgg|gtt|cgC|CAa|gct|ccT|GG-3′(SEQ ID NO: 31) ! ON = 82 bases ! CDR2(ON-R2V1vg)                               5′-ggt|ttg|gag|tgg|gtt|tct|-          <2>|atc|<2>|<3>|tct|ggt|ggc|<1>|act|<1>|-                  tat|gct|gac|tcc|gtt|aaa|gg-3′ (SEQ ID NO: 32)! ON = 68bases, CDR2 = 17 AA(ON-R2top) 5′-ct|tgg|gtt|cgC|CAa|gct|ccT|GGt|aaa|ggt|ttg|gag|tgg|gtt|tct-3′           (SEQ ID NO: 33) (ON-R2bot)[RC]5′-tat|gct|gac|tcc|gtt|aaa|ggt|-           cgc|ttc|act|atc|TCT|AGA|ttcctgtcac-3′ (SEQ ID NO: 34)!XbaI plus 10 bases of scab(ON-R2V2vg)                               5′-ggt|ttg|gag|tgg|gtt|tct|-          <1>|atc|<4>|<1>|<1>|ggt|<5>|<1>|<1>|<1>|-                  tat|gct|gac|tcc|gtt|aaa|gg-3′ (SEQ ID NO: 35)! ON = 68bases, CDR2 = 17 AA ! <4> = DINSWY, equimolar ! <5> = SGDN, equimolar(ON-R2V3vg)                               5′-ggt|ttg|gag|tgg|gtt|tct|-          <1>|atc|<4>|<1>|<1>|ggt|<5>|<1>|<1>|-                  tat|aac|cct|tcc|ctt|aag|gg-3′ (SEQ ID NO: 36)! ON = 65bases, CDR2 = 16 AA (ON-R2bo3)[RC] 5′-tat|aac|cct|tcc|ctt|aag|ggt|-           cgc|ttc|act|atc|TCT|AGA|ttcctgtcac-3′ (SEQ ID NO: 37)!XbaI plus 10 bases of scab(ON-R2V4vg)                               5′-ggt|ttg|gag|tgg|gtt|tct|-          <1>|atc|<8>|agt|<1>|<1>|<1>|ggt|ggt|act|act|<1>                  tat|gcc|gct|tcc|gtt|aag|gg-3′ (SEQ ID NO: 38)! ON = 74bases, CDR2 = 19 AA (ON-R2bo4)[RC] 5′-tat|gcc|gct|tcc|gtt|aag|ggt|-           cgc|ttc|act|atc|TCT|AGA|ttcctgtcac-3′ (SEQ ID NO: 39) !XbaI plus 10 bases of scab

TABLE 25P Lengths of CDRs in 285 human kappa chains 0 1 2 3 4 5 6 7 8 910 11 12 13 14 15 16 17 18 19 CDR1 0 0 0 0 0 0 0 0 0 0 0 154 73 3 0 0 2827 0 0 CDR2 0 0 0 0 0 0 0 285 0 0 0 0 0 0 0 0 0 0 0 0 CDR3 0 5 0 0 1 0 32 28 166 63 12 1 1 0 0 0 0 0 1

TABLE 26P Tally of kappa types: V and J V genes: O12 59 O2 0 O18 0 O8 0A20 0 A30 0 L14 0 L1 2 L15 0 L4 2 L18 0 L5 4 L19 0 L8 4 L23 0 L9 1 L24 0L11 4 L12 8 O11 10 O1 0 A17 5 A1 0 A18 3 A2 0 A19 13 A3 0 A23 4 A27 79A11 26 L2 28 L16 0 L6 11 L20 0 L25 0 B3 22 B2 0 A26 0 A10 0 A14 0 JH# 12 3 4 5 tally 105 64 29 78 9

TABLE 27P Names of Kappa chains analyzed AB022651 AB022653 AB022654AB022656 AF007572 AF021036 AF103499 AF103500 AF103527 AF103873 AF107244AF107245 AF107246 AF107247 AF115361 AF165099 AF165101 AF165103 AF165108AF165110 AF165111 AF184763 AF184767 hsa004955 hsa004956 hsa011133HSA241367 HSA241375 HSA388639 HSA388640 HSA388641 HSA388642 HSA388643HSA388644 HSA388645 HSA388646 HSA388647 HSA388648 HSA388650 HSA388651HSA388652 HSA388653 HSA388654 HSA388655 HSA388656 HSA388657 hsew1vkhsew3vk hsew4vk hsigdpk13 hsigg1kl HSIGGVKA hsigk123 hsigk319 hsigklc14hsigklc28 hsigklc5 hsigklg31 hsigklv01 hsigklv02 hsigklv03 hsigklv04hsigklv05 hsigklv06 hsigklv07 hsigklv09 hsigklv10 hsigklv12 hsigklv13hsigklv14 hsigklv15 hsigklv16 hsigklv17 hsigklv18 hsigklv19 hsigklv20hsigklv21 hsigklv22 hsigklv23 hsigklv24 hsigklv25 hsigklv27 hsigklv28hsigklv29 hsigklv31 hsigklv32 hsigklv33 hsigklv34 hsigklv35 hsigklv36hsigklv37 hsigklv38 hsigklv39 hsigklv40 hsigklv41 hsigklv42 hsigklv43hsigklv44 hsigklv45 hsigklv46 hsigklv49 hsigklv50 hsigklv51 hsigklv52hsigklv53 hsigklv54a hsigklv56 hsigklv57 hsigklv58 hsigklv59 hsigklv60hsigklv61 hsigklv62 hsigklv63 hsigklv65 hsigklv66 hsigklv68 hsigklv69hsigklv71 hsigkvba hsigkvbb hsigkvbc hsigkvbd hsigkvbe hsigkvbfhsigkvc01 hsigkvc03 hsigkvc06 hsigkvc11 hsigkvc12 hsigkvc20 hsigkvc23hsigkvc27 hsigkvc29 hsigrklc hsikcvjp1 hsikcvjp2 hsikcvjp3 hsikcvjp6hsikcvjp7 hsld110vl hsld117vl hsld128vl hsld140vl hsld152vl hsld184vlhsld198vl hsld24vl hsmbcl1k1 hsmbcl1k2 hsmbcl2k2 hsmbcl5k4 hss10avlhss17bvl hss1a15vl HSU44792 HSU44794 HSU94422 hsz84852 hsz84853humigk1dm humigk3am humigk3bm humigk3cm humigkacoa humigkacob humigkacochumigkacoe humigkacof humigkb1aa humigkb1ab humigkb1ac humigkvrahumigkvrb humigkvrc humigkvrd humigkvre humigkvrg humigkvrh humigkvrihumigkx humigky1 humigky2 humigky4 humigky5 humigky6 humigl3ac humikchumikca humikcad humikcaf humikcag humikcah humikcai humikcaj humikcalhumikcam humikcan humikcas humikcau humikcav humikcaw humikcax humikcayhumikcaz humikcb humikcba humikcbb humikcbc humikcbd humikcbe humikcbfhumikcbg humikcbh humikcbi humikcbj humikcbl humikcbm humikcbn humikcbohumikcbp humikcbq humikcbs humikcbt humikcbu humikcbv humikcbw humikcbxhumikcbz humikcc humikcca humikccb humikccc humikccd humikcce humikccfhumikccg humikcch humikcci humikccj humikcck humikcco humikccp humikccqhumikccr humikccs humikcct humikccu humikccv humikccw humikcd humikcfhumikcg humikch humikci humikck humikcm humikcn humikco humikcp humikcqhumikcr humikcs humikct humikcu humikcv humikcva humikcvb humikcvchumikcvd humikcve humikcvf humikcvg humikcvh humikcvi humikcvj humikcwhumikcx humikcy humikcz S46248 S82746 S82747 SU96396 SU96397

TABLE 28P AA types seen in 154 kappa sequences having CDR1 of length 11Tally A C D E F G H I K L M N P Q R S T V W Y 1 11 143 R 2 148 1 2 2 1 A3 152 2 S 4 1 3 3 147 Q 5 12 1 27 7 3 99 4 1 S 6 1 81 1 71 V 7 2 4 18 51 2 9 12 97 3 1 S 8 3 5 1 2 1 31 1 10 87 12 1 S 9 2 7 10 1 6 29 1 8 1377 Y 10 2 150 1 1 L 11 96 4 2 46 2 1 3 A

TABLE 30P Synthetic Kappa light chain gene ! ! !A27::JH1 with all CDRs replaced by stuffers. !Each stuffer contains at least one stop codon and a !restriction site that will be unique within the diversity vector. !    1 GAGGACCATt GGGCCCC                 ctccgagact !    Scab...... Eco0109I !                ApaI.!----------------------------------- !    28         CTCGAG    cgca !            XhoI.. !----------------------------------- !   38 acgcaatTAA TGTgagttag ctcactcatt aggcacccca ggcTTTACAc tttatgcttc!            ..−35..         Plac                    ..−10.!----------------------------------- !   98 cggctcgtat gttgtgtgga attgtgagcg gataacaatt tc!----------------------------------- !   140 acacagga aacagctatgac!----------------------------------- !  160 catgatta cgCCAAGCTT TGGagccttt tttttggaga ttttcaac (SEQ ID NO: 54)!                PflMI....... !                Hind3.!----------------------------------- ! !   M13 III signal sequence (AA seq)---------------------------> !     1   2   3   4   5   6   7   8   9  10  11  12  13  14  15 !     M   K   K   L   L   F   A   I   P   L   V   V   P   F   Y  206 gtg aag aag ctc cta ttt gct atc ccg ctt gtc gtt ccg ttt tac!----------------------------------- ! !    --Signal-->FR1-------------------------------------------> !    16  17  18  19  20  21  22  23  24  25  26  27  28  29  30 !     S   H   S   A   Q   S   V   L   T   Q   S   P   G   T   L  251|agc|cat|aGT|GCA|Caa|tcc|gtc|ctt|act|caa|tct|cct|ggc|act|ctt| !             ApaLI... !----------------------------------- ! !   ----- FR1 ------------------------------------->| CDR1------> !    31  32  33  34  35  36  37  38  39  40  41  42  43  44  45 !     S   L   S   P   G   E   R   A   T   L   S   C   R   A   S    (SEQ ID NO: 55)     |tcG|CTA|AGC|CCG|GGt|gaa|cgt|gct|acC|TTA|AGt|tgc|cgt|gct|tcc| (SEQ ID NO: 54; Cont'd)) !      EspI.....                       AflII... !               XmaI....! !---------------------------------- ! For CDR1: ! <1>ADEFGHIKLMNPQRSTVWY equimolar ! <2>S(0.2) ADEFGHIKLMNPQRTVWY (0.044 each) ! <3>Y(0.2) ADEFGHIKLMNPQRSTVW (0.044 each) !In a preferred embodiment, we omit codon 52 in vgDNA for CDR1. ! !         ------- CDR1 --------------------->|--- FR2 ---------------> !             <1>     <2> <2> xxx <3> !         46  47  48  49  50  51  52  53  54  55  56  57  58  59  60 !          Q   S   V   S   S   S   Y   L   A   W   Y   Q   Q   K   P          |cag|tct|gtt|tcc|tct|tct|tat|ctt|gct|tgg|tat|caa|cag|aaA|CCT|!                                                               SexAI...! !---------------------------------- ! For CDR2: ! <1>ADEFGHIKLMNPQRSTVWY equimolar ! <2>S(0.2) ADEFGHIKLMNPQRTVWY (0.044 each) ! <4>A(0.2) DEFGHIKLMNPQRSTVWY (0.044 each) !         ----- FR2 ------------------------->|------- CDR2 ----------> !                                             <1>         <2>     <4> !         61  62  63  64  65  66  67  68  69  70  71  72  73  74  75 !          G   Q   A   P   R   L   L   I   Y   G   A   S   S   R   A          |GGT|caG|GCG|CCg|cgt|tta|ctt|att|tat|ggt|gct|tct|tcc|cgc|gct|!   SexAI....   KasI.... (CDR1 installed as AflII-(SexAI or KasI) cassette.)! !---------------------------------- ! !     CDR2-->|--- FR3-----------------------------------------------> !         <1> !         76  77  78  79  80  81  82  83  84  85  86  87  88  89  90 !          T   G   I   P   D   R   F   S   G   S   G   S   G   T   D |        |act|gGG|ATC|CCG|GAC|CGt|ttc|tct|ggc|tct|ggt|tca|ggt|act|gac| !              BamHI... !                      RsrII..... !(CDR2 installed as (SexAI or KasI) to (BamHI or RsrII) cassette.)!---------------------------------- ! !        ------ FR3 ------------------------------------------------> !         91  92  93  94  95  96  97  98  99 100 101 102 103 104 105 !          F   T   L   T   I   S   R   L   E   P   E   D   F   A   V  477     |ttt|acc|ctt|act|att|TCT|AGA|ttg|gaa|cct|gaa|gac|ttc|gct|gtt|!                              XbaI... !!---------------------------------- ! !        ----------->|----CDR3-------------------------->|-----FR4---> !                             <3> <1> <1> <1>     <1> !        106 107 108 109 110 111 112 113 114 115 116 117 118 119 120 !          Y   Y   C   Q   Q   Y   G   S   S   P   E   T   F   G   Q          |tat|tat|tgC|CAa|cag|taT|GGt|tct|tct|cct|gaa|act|ttc|ggt|caa|!                    BstXI........... !!---------------------------------- ! !        -----FR4------------------->|      <------- Ckappa ------------!         121 122 123 124 125 126 127        128 129 130 131 132 133 134!           G   T   K   V   E   I   K         R   T   V   A   A   P   S  510     |ggt|aCC|AAG|Gtt|gaa|atc|aag|     |CGT|ACG|gtt|gcc|gct|cct|agt!               StyI....                     BsiWI.. ! !(CDR3 installed as XbaI to (StyI or BsiWI) cassette.) ! !        135 136 137 138 139 140 141 142 143 144 145 146 147 148 149 !         V   F   I   F   P   P   S   D   E   Q   L   K   S   G   T  552    |gtg|ttt|atc|ttt|cct|cct|tct|gac|gaa|CAA|TTG|aag|tca|ggt|act| !                                            MfeI... ! !        150 151 152 153 154 155 156 157 158 159 160 161 162 163 164 !         A   S   V   V   C   L   L   N   N   F   Y   P   R   E   A  597    |gct|tct|gtc|gta|tgt|ttg|ctc|aac|aat|ttc|tac|cCT|CGT|Gaa|gct| !                                                     BssSI... ! !        165 166 167 168 169 170 171 172 173 174 175 176 177 178 179 !         K   V   Q   W   K   V   D   N   A   L   Q   S   G   N   S  642    |aaa|gtt|cag|tgg|aaa|gtc|gat|aAC|GCG|Ttg|cag|tcg|ggt|aac|agt| !                                     MluI.... ! !        180 181 182 183 184 185 186 187 188 189 190 191 192 193 194 !         Q   E   S   V   T   E   Q   D   S   K   D   S   T   Y   S  687    |caa|gaa|tcc|gtc|act|gaa|cag|gat|agt|aag|gac|tct|acc|tac|tct| !!         195 196 197 198 199 200 201 202 203 204 205 206 207 208 209 !         L   S   S   T   L   T   L   S   K   A   D   Y   E   K   H  732    |ttg|tcc|tct|act|ctt|act|tta|tca|aag|gct|gat|tat|gag|aag|cat| !!         210 211 212 213 214 215 216 217 218 219 220 221 222 223 224 !         K   V   Y   A   C   E   V   T   H   Q   G   L   S   S   P  777    |aag|gtc|tat|GCt|TGC|gaa|gtt|acc|cac|cag|ggt|ctG|AGC|TCc|cct| !                                                      SacI.... ! !        225 226 227 228 229 230 231 232 233 234 !         V   T   K   S   F   N   R   G   E   C   .   . (SEQ ID NO: 332)  822    |gtt|acc|aaa|agt|ttc|aaC|CGT|GGt|gaa|tgc|taa|tag GGCGCGCC !                              DsaI....                  AscI....  !                                                         BssHII  866    acgcatctctaa GCGGCCGC aacaggaggag               (SEQ ID NO: 333)!                     NotI.... !                      EagI..

TABLE 31P Tally of 285 CDR2s of length 7 in human kappa Tally A C D E FG H I K L M N P Q R S T V W Y 1 51 62 7 95 1 11 15 2 1 2 6 6 3 22 1 x 2225 18 5 5 2 1 1 3 16 9 A 3 2 9 1 2 267 2 1 1 S 4 2 1 5 4 9 1 77 4 93 802 7 Sx 5 1 2 80 200 2 R 6 162 7 36 4 4 1 3 3 63 2 Ax 7 5 1 3 1 1 2 2 1125 144 x

TABLE 32P Tally of 166 CDR3s of length 9 from human kappa. Tally A C D EF G H I K L M N P Q R S T V W Y 1 4 8 21 131 1 1 Q 2 1 9 2 1 153 Q 3 144 4 3 6 4 1 1 3 21 16 3 4 82 Yx 4 1 9 1 2 37 4 2 2 15 1 33 2 20 7 1 29 x5 2 2 6 3 4 5 3 28 17 7 65 19 1 1 3 x 6 7 1 11 2 3 8 1 4 3 41 33 5 28 19x 7 1 2 6 146 2 2 5 2 P 8 2 4 1 2 21 7 3 5 1 38 7 4 25 1 3 1 16 25 x 9 32 1 1 2 157 T

TABLE 33P lengths of CDRs in 93 human lambda chains 0 1 2 3 4 5 6 7 8 910 11 12 13 14 15 16 17 18+ CDR1 0 0 0 0 0 0 0 0 0 0 0 23 7 15 46 0 0 02 CDR2 5 0 0 1 0 0 0 80 2 0 0 1 4 0 0 0 0 0 1 CDR3 0 0 0 0 0 0 0 0 1 1628 27 6 1 0 4 6 4 0

TABLE 34P Tally of 46 CDR1s of length 14 from human lambda chains TallyA C D E F G H I K L M N P Q R S T V W Y 1 2 2 1 41 T 2 43 3 G 3 2 1 1 636 TGx 4 1 45 S 5 5 1 40 S 6 39 1 4 2 DNx 7 8 1 37 V 8 1 42 2 1 G 9 4 135 1 2 3 TGx 10 1 1 3 1 2 38 Yx 11 4 1 35 6 DNx 12 3 1 2 1 1 2 36 Yx 131 2 43 V 14 1 4 41 S

TABLE 35P Synthtic human lambda-chain gene

TABLE 36P Tally of 23 CDR1s of length 11 from human lambda chains TallyA C D E F G H I K L M N P Q R S T V W Y 1 1 6 10 6 x 2 1 1 21 G 3 15 1 7DNx 4 2 1 1 3 7 1 8 X 5 7 16 L 6 11 1 2 8 1 X 7 1 1 1 2 2 1 14 1 X 8 110 1 1 1 2 7 X 9 2 6 15 Yx 10 11 1 11 X 11 3 7 9 2 2 X

TABLE 37P Tally of 80 CDR2s of length 7 from human lambda chains Tally AC D E F G H I K L M N P Q R S T V W Y 1 1 14 32 1 13 3 1 4 5 1 2 3 X 218 2 8 16 2 34 X 3 1 2 1 31 39 4 2 X 4 6 4 1 14 1 41 8 1 1 2 1 DNx 5 1 178 R 6 1 77 2 P 7 2 78 S

TABLE 38P Tally of 27 CDR3s of length 11 from human lambda chains TallyA C D E F G H I K L M N P Q R S T V W Y 1 4 5 6 5 4 3 X 2 3 1 2 14 5 2Sx 3 1 7 13 6 X 4 19 2 1 1 4 DNx 5 1 4 2 2 2 1 13 2 X 6 1 3 1 21 1 S 7 17 12 1 4 2 X 8 2 1 10 1 6 6 1 X 9 3 1 8 10 3 1 1 X 10 1 4 1 1 1 3 1 1 65 3 X 11 2 25 V

TABLE 40P  Synthetic Kappa light chain gene with stuffers

TABLE 41P Variegated DNA for kappa chains!---------------------------------------------------------------- !Kappa chains ! For CDR1: ! <1> ADEFGHIKLMNPQRSTVWY equimolar ! <2>S(0.2) ADEFGHIKLMNPQRTVWY (0.044 each) ! <3>Y(0.2) ADEFGHIKLMNPQRSTVW (0.044 each) ! <4>A(0.2) DEFGHIKLMNPQRSTVWY (0.044 each)(Kalvg600)                         5′-gct|acC|TTA|AGt|tgc|cgt|gct|tcc|cag-      |<1>|gtt|<2>|<2>|    <3>|ctt|gct|tgg|tat|caa|cag|aaA|CC-3′ (SEQ ID NO: 66)(Ka2vg650)      5′-caG|GCG|CCg|cgt|tta|ctt|att|tat|<1>|gct|tct|<2>|cgc|<4>|-                  |<1>|gGG|ATC|CCG|GAC|CGt|ttc|tct|ggt|tctcacc-3′(SEQ ID NO: 71)(Ka3vg670) 5′-                                            gac|ttc|gct|gtt|-             |tat|tat|tgC|CAa|cag|<3>|<1>|<1>|<1>|cct|<1>|act|ttc|ggt|caa|-             |ggt|aCC|AAG|Gtt|g-3′ (SEQ ID NO: 77)

TABLE 42P Variegated DNA for lambda chains !------------------------ !For CDR1, ! <1> = 0.27 T, 0.27 G, 0.027 {ADEFHIKLMNPQRSVWY} no C ! <2> =0.27 D, 0.27 N, 0.027 {AEFGHIKLMPQRSTVWY} no C ! <3> =0.36 Y, 0.0355{ADEFGHIKLMNPQRSTVW}        no C ! <4> =equimolar {ADEFGHIKLMNPQRSTVWY} no C ! <5> =0.36 S, 0.0355{ADEFGHIKLMNPQRTVWY} no C(Lm1vg710) 5′-gt|atc|act|att|tct|TGT|ACA|ggt|<1>|tct|tct|<2>|gtt|ggc|-       |<1>|<3>|<2>|<3>|gtt|tct|tgg|tat|caa|caa|caC|CC-3′(SEQ ID NO: 83) !------------------------------------------------(Lm2vg750)                              5′-G|CCg|aag|ttg|atg|atc|tac|-   <4>|<4>|<4>|<2>|cgt|cct|tct|ggt|gtc|agc|aat|c-3′      (SEQ ID NO: 88)(Lm3vg817) 5′-                         gac|gag|gct|gac|tac|tat|tgt|-       |<4>|<5>|<4>|<2>|<4>|tct|<4>|<4>|<4>|<4>|gtc|ttc|ggc|ggt|GGT|-      |ACC|aaa|ctt|ac-3′     (SEQ ID NO: 93)!----------------------------------------------------------------

TABLE 43P Constant DNA for Synthetic Library ! CDR3 library components(Ctop25) 5′-gctctggtcaa C|TTA|AGg|gct|gag|g-3′ (SEQ ID NO: 58)(CtprmA) 5′-gctctggtcaa C|TTA|AGg|gct|gag|gac- !                      AflII...            |acc|gct|gtc|tac|tac|tgc|gcc-3′    (SEQ ID NO: 59) !(CBprmB)[RC]5′-|tac|ttc|gat|tac|ttg|ggc|caa|GGT|ACC|ctG|GTC|ACC|tcgctccacc-3′(SEQ ID NO: 60) !                                                     BstEII . . .(CBot25)[RC]                            5′-|GGT|ACC|ctG|GTC|ACC|tcgctccacc-3′(SEQ ID NO: 61)!---------------------------------------------------------------- !Kappa chains (Ka1Top610) 5′-ggtctcagtt-            G|CTA|AGC|CCG|GGt|gaa|cgt|gct|acC|TTA|AGt|tgc|cgt|gct|tcc|cag-3′  (SEQ ID NO: 62) (Ka1STp6l5) 5′-ggtctcagtt-            G|CTA|AGC|CCG|GGt|g-3′ (SEQ ID NO: 63) (Ka1Bot620) [RC]           5′-ctt|gct|tgg|tat|caa|cag|aaA|-                    CCt|GGT|caG|GCG|CC aagtcgtgtc-3′  (SEQ ID NO: 64)(KalSB625)  [RC] 5′-cct |GGT|caG|GCG|CC|aagtcgtgtc-3′ (SEQ ID NO: 65) !(Ka2Tshort657) 5′-cacgagtcctA|CCT|GGT|-                    caG|GC-3′(SEQ ID NO: 68) (Ka2Tlong655)  5′-cacgagtcctA|CCT|GGT|-                   caG|GCG|CCg|cgt|tta|ctt|att|tat-3′ (SEQ ID NO: 69)(Ka2Bshort660) [RC] 5′-           |GAC|CGt|ttc|tct|ggt|tctcacc-3′(SEQ ID NO: 70)!-----------------------------------------------------------------(Ka3Tlon672)5′-       gacgagtcct  TCT|AGA|ttg|gaa|cct|gaa|gac|ttc|gct|gtt|-             |tat|tat|tgC|CAa|c|-3′   (SEQ ID NO: 72)(Ka3BotL682)                                       [RC]5′-act|ttc|ggt|caa|-              |ggt|aCC|AAG|Gtt|gaa|atc|aag|     |CGT|ACG| tcacaggtgag-3′  (SEQ ID NO: 73)(Ka3Bsho694) [RC]5′-          gaa|atc|aag|    |CGT|ACG| tcacaggtgag-3′(SEQ ID NO: 74)!-----------------------------------------------------------------(Lm1TPri75) 5′-gacgagtcct GG|TcA|CCt|GGT|-3′ (SEQ ID NO: 78)(Lm1TLo715) 5′-gacgagtcct GG|TcA|CCt|GGT|-         caa|agt|atc|act|att|tct|TGT|ACA|ggt-3′ (SEQ ID NO: 79)(Lm1BLo724)[RC] 5′-gtt|tct|tgg|tat|caa|caa|caC|CCG|GGc|aaG|GCG|-         AGA TCT  tcacaggtgag-3′ (SEQ ID NO: 80) (Lm1BSh737) [RC]5′-                                Gc|aaG|GCG -         AGA TCT  tcacaggtgag-3′ (SEQ ID NO: 81)!-------------------------------------------------(Lm2TSh757) 5′-gagcagagga C|CCG|GGc|aaG|GC-3′ (SEQ ID NO: 84)(Lm2TLo753) 5′-gagcagagga C|CCG|GGc|aaG|GCG|CCg|aag|ttg|atg|atc|tac|-3′(SEQ ID NO: 85) (Lm2BLo762)[RC]5′-cgt|cct|tct|ggt|gtc|agc|aat|cgt|ttc|TCC|GGA|tcacaggtgag-3′(SEQ ID NO: 86) (Lm2BSh765)[RC]5′-                            cgt|ttc|TCC|GGA|tcacaggtgag-3′(SEQ ID NO: 87) !-------------------------------------------------(Lm3TSh822)         5′-CTG|CAG|gct|gaa|gac|gag|gct|gac             -3′(SEQ ID NO: 89)(Lm3TLo819)         5′-CTG|CAG|gct|gaa|gac|gag|gct|gac|tac|tat|tgt|-3′(SEQ ID NO: 90) (Lm3BLo825) [RC]                            5′-gtc|ttc|ggc|ggt|GGT|-      |ACC|aaa|ctt|act|gtc|ctc|gGT|CAA|CCT|aAG|G acacaggtgag-3′(SEQ ID NO: 91) (Lm3BSh832) [RC]  5′-       c|gGT|CAA|CCT|aAG|G acacaggtgag-3′ (SEQ ID NO: 92)

TABLE 48PSynthtic human lambda-chain gene with stuffers in place of CDRs

TABLE 50P 3-23::CDR3::JH4 Stuffers in place of CDRs

1.-43. (canceled)
 44. A library, comprising a first set of variegatedDNA molecules encoding a collection of antibody heavy chains (HC),wherein each comprises a CDR1 region, a CDR2 region, and a CDR3 region,and wherein at least a heavy chain portion of the collection comprises aplurality of components that contain HC CDR3 regions, the componentsbeing selected from the group consisting of: (i) YYCA21111YFDYWG (SEQ IDNO:6), wherein 1 is any amino acid residue except C, and 2 is a mixtureof K and R; (ii) YYCA2111111YFDYWG (SEQ ID NO:7), wherein 1 is any aminoacid residue except C, and 2 is a mixture of K and R; (iii)YYCA211111111YFDAYTG (SEQ ID NO:8), wherein 1 is any amino acid residueexcept C, and 2 is a mixture of K and R; (iv) YYCAR111S2S3111YFDYWG (SEQID NO:9), wherein 1 is any amino acid residue except C, 2 is a mixtureof S and G, and 3 is a mixture of Y and W; (v) YYCA2111CSG11CY1YFDYWG(SEQ ID NO:10), wherein 1 is any amino acid residue except C, and 2 is amixture of K and R; (vi) YYCA211S1TIFG11111YFDYWG (SEQ ID NO:11),wherein 1 is any amino acid residue except C, and 2 is a mixture of Kand R; (vii) YYCAR111YY2S3344111YFDYWG (SEQ ID NO:12), wherein 1 is anyamino acid residue except C, 2 is D or S, and 3 is a mixture of S and G;(viii) YYCAR1111YC2231CY111YFDYWG (SEQ ID NO:13), wherein 1 is any aminoacid residue except C, 2 is a mixture of S and G, and 3 is a mixture ofT, D and G; and (ix) a mixture of any of (i) to (viii) set forth above.45. The library of claim 44, wherein: the complexity of component (i) is2×10⁵, the complexity of component (ii) is 9.4×10⁷, the complexity ofcomponent (iii) is 3.4×10¹⁰, the complexity of component (iv) is1.9×10⁸, the complexity of component (v) is 9.4×10⁷, the complexity ofcomponent (vi) is 1.7×10¹⁰, the complexity of component (vii) is3.8×10⁸, and the complexity of component (viii) is 2.0×10¹¹.
 46. Thelibrary of claim 44, wherein: in one or more of components (i), (ii),(iii), (v), and (vi), 1 is (a) an equimolar mixture of amino acidresidues A, D, E, F, G, H, I, K, L, M, N, P, Q, R, S, T, V, W and Y; or(b) a mixture of 0.095 Y, 0.095 G, and 0.048 each of A, D, E, F, H, I,K, L, M, N, P, Q, R, S, T, V, and W; and 2 is an equimolar mixture of Kand R; in (iv), 1 is (a) an equimolar mixture of amino acid residues A,D, E, F, G, H, I, K, L, M, N, P, Q, R, S, T, V, W and Y; or (b) amixture of 0.095 Y, 0.095 G, and 0.048 each of A, D, E, F, H, I, K, L,M, N, P, Q, R, S, T, V, and W; 2 is an equimolar mixture of S and G; and3 is an equimolar mixture of Y and W; in (vii), 1 is (a) an equimolarmixture of amino acid residues A, D, E, F, G, H, I, K, L, M, N, P, Q, R,S, T, V, W and Y; or (b) a mixture of 0.095 Y, 0.095 G, and 0.048 eachof A, D, E, F, H, I, K, L, M, N, P, Q, R, S, T, V, and W; 2 is anequimolar mixture of D and G; and 3 is an equimolar mixture of S and G;or in (viii), 1 is (a) an equimolar mixture of amino acid residues A, D,E, F, G, H, I, K, L, M, N, P, Q, R, S, T, V, W and Y; or (b) a mixtureof 0.095 Y, 0.095 G, and 0.048 each of A, D, E, F, H, I, K, L, M, N, P,Q, R, S, T, V, and W; 2 is an equimolar mixture of S and G; and 3 is anequimolar mixture of T, D, and G.
 47. The library of claim 44, whereincomponents (i) through (viii) are present in the library in thefollowing proportions: (i) 0.10, (ii) 0.14, (iii) 0.25, (iv) 0.13, (v)0.13, (vi) 0.11, (vii) 0.04, and (viii) 0.10.
 48. The library of claim44, wherein components (i) through (viii) are present in the library inthe following proportions: (i) 0.02, (ii) 0.14, (iii) 0.25, (iv) 0.14,(v) 0.14, (vi) 0.12, (vii) 0.08, and (viii) 0.11.
 49. The library ofclaim 44, wherein the heavy chain portion further comprises a pluralityof HC CDR1 regions selected from the group consisting of: (1)<1>₁Y₂<1>₃M₄<1>₅ (SEQ ID NO:100), wherein <1> is an equimolar mixture ofeach of amino acid residues A, D, E, F, G, H, I, K, L, M, N, P, Q, R, S,T, V, W, and Y; (2) (S/T)₁(S/G/X)₂(S/G/X)₃Y₄Y₅W₆(S/G/X)₇ (SEQ IDNO:101), wherein (SIT) is a 1:1 mixture of S and T residues, (S/G/X) isa mixture of 0.2025 S, 0.2025, G and 0.035 of each of amino acidresidues A, D, E, F, H, I, K, L, M, N, P, Q, R, T, V, W, and Y; (3)V₁S₂G₃G₄S₅I₆S₇<<1>₈<1>₉<1>₁₀Y₁₁Y₁₂W₁₃<1>₁₄ (SEQ ID NO:1), wherein <1> isan equimolar mixture of each of amino acid residues A, D, E, F, G, H, I,K, L, M, N, P, Q, R, S, T, V, W, and Y; and (4) a mixture of any of (1)to (3) set forth above.
 50. The library of claim 44, wherein the heavychain portion further comprises a plurality of HC CDR2 regions selectedfrom the group consisting of: (1) <2>I<2><3>SGG<1>T<1>YADSVKG (SEQ IDNO:2), wherein <1> is an equimolar mixture of each of amino acidresidues A, D, E, F, G, H, I, K, L, M, N, P, Q, R, S, T, V, W, and Y;<2> is an equimolar mixture of each of amino acid residues Y, R, W, V,G, and S; and <3> is an equimolar mixture of each of amino acid residuesP, S, and G or an equimolar mixture of P and S; (2)<1>I<4><1><1><G><5><1><1>-<1>YADSVKG (SEQ ID NO:3), wherein <1> is anequimolar mixture of each of amino acid residues A, D, E, F, G, H, I, K,L, M, N, P, Q, R, S, T, V, W, and Y; <4> is an equimolar mixture ofresidues D, I, N, S, W, Y; and <5> is an equimolar mixture of residuesS, G, D and N; (3) <1>I<4><1><1>G<5><1><1>YNPSLKG (SEQ ID NO:4), wherein<1> is an equimolar mixture of each of amino acid residues A, D, E, F,G, H, I, K, L, M, N, P, Q, R, S, T, V, W and Y; and <4> and <5> are asdefined above; (4) <1>I<8>S<1><1><1>GGYY<1>YAASVKG (SEQ ID NO:5),wherein <1> is an equimolar mixture of each amino acid residues A, D, E,F, G, H, I, K, L, M, N, P, Q, R, S, T, V, W and Y; <8> is 0.27 R and0.027 of each of ADEFGHIKLMNPQSTVWY; and (5) a mixture of any of (1) to(4) set forth above.
 51. The library of claim 49, wherein the heavychain portion further comprises a plurality of HC CDR2 regions selectedfrom the group consisting of: (1) <2>I<2><3>SGG<1>T<1>YADSVKG (SEQ IDNO:2), wherein <1> is an equimolar mixture of each of amino acidresidues A, D, E, F, G, H, 1, K, L, M, N, P, Q, R, S, T, V, W, and Y;<2> is an equimolar mixture of each of amino acid residues Y, R, W, V,G, and S; and <3> is an equimolar mixture of each of amino acid residuesP, S, and G or an equimolar mixture of P and S; (2)<1>I<4><1><1><G><5><1><1>-<1>YADSVKG (SEQ ID NO:3), wherein <1> is anequimolar mixture of each of amino acid residues A, D, E, F, G, H, I, K,L, M, N, P, Q, R, S, T, V, W, and Y; <4> is an equimolar mixture ofresidues D, I, N, S, W, Y; and <5> is an equimolar mixture of residuesS, G, D and N; (3) <1>I<4><1><1>G<5><1><1>YNPSLKG (SEQ ID NO:4), wherein<1> is an equimolar mixture of each of amino acid residues A, D, E, F,G, H, I, K, L, M, N, P, Q, R, S, T, V, W and Y; and <4> and <5> are asdefined above; (4) <1>I<8>S<1><1><1>GGYY<1>YAASVKG (SEQ ID NO:5),wherein <1> is an equimolar mixture of each amino acid residues A, D, E,F, G, H, I, K, L, M, N, P, Q, R, S, T, V, W and Y; <8> is 0.27 R and0.027 of each of A, D, E, F, G, H, I, K, L, M, N, P, Q, S, T, V, W, andY; and (5) a mixture of any of (1) to (4) set forth above.
 52. Thefocused library according to claim 49, wherein the HC CDR1s (1), (2) and(3) regions are present in the library in the ratio 0.80:0.17:0.02. 53.The focused library according to claim 50, wherein a mixture of HC CDR2s(1)/(2) (equimolar), (3) and (4) are present in the library in a ratioof 0.54:0.43:0.03.
 54. The library of claim 44, further comprising asecond set of variegated DNA molecules encoding a collection of antibodylight chains (LC), wherein each comprises a CDR1 region, a CDR2 region,and a CDR3 region.
 55. The library of claim 54, wherein at least a lightchain portion of the collection are kappa light chains, each of whichcomprises a LC_(κ) CDR1 region, a LC_(κ) CDR2 region, and a LC_(κ) CDR3region.
 56. The library of claim 55, wherein the light chain portioncomprises a plurality of LC_(κ) CDR3 regions selected from the groupconsisting of: (1) QQ<3><1><1><1>P<1>T (SEQ ID NO:16), wherein <1> is anequimolar mixture of amino acid residues ADEFGHIKLMNPQRSTVWY; and <3> is0.2 Y and 0.044 each of A, D, E, F, G, H, I, K, L, M, N, P, Q, R, T, V,and W; (2) QQ33111P (SEQ ID NO:103), wherein 1 and 3 are as defined in(1) above; (3) QQ3211PP1T (SEQ ID NO:17), wherein 1 and 3 are as definedin (1) above and 2 is 0.2 S and 0.044 each of A, D, E, F, G, H, I, K, L,M, N, P, Q, R, T, V, W, and Y; and (4) a mixture of any of (1) to (3)set forth above.
 57. The library of claim 56, wherein the light chainportion further comprises a plurality of LC_(κ) CDR1 regions selectedfrom the group consisting of: (1) RASQ<1>V<2><2><3>LA (SEQ ID NO:14),wherein <1> is an equimolar mixture of amino acid residues A, D, E, F,G, II, I, K, L, M, N, P, Q, R, S, T, V, W, Y; <2> is 0.2 S and 0.044 ofeach of A, D, E, F, G, H, I, K, L, M, N, P, Q, R, T, V, W, Y; and <3> is0.2Y and 0.044 each of A, D, E, F, G, H, I, K, L, M, N, P, Q, R, T, V, Wand S; and (2) RASQ<1>V<2><2><2><3>LA (SEQ ID NO:15); wherein <1>, <2>,and <3> are as defined in (1) above; and (3) a mixture of (1) and (2)set forth above.
 58. The library of claim 56, wherein the light chainportion further comprises a plurality of LC_(κ) CDR2 regions<1>AS<2>R<4><1> (SEQ ID NO:102), wherein <1> is an equimolar mixture ofamino acid residues A, D, E, F, G, H, I, K, L, M, N, P, Q, R, S, T, V,W, and Y; <2> is 0.2 S and 0.044 of each of A, D, E, F, G, H, I, K, L,M, N, P, Q, R, T, V, W, and Y; and <4> is 0.2 A and 0.044 each of D, E,F, G, H, I, K, L, M, N, P, Q, R, S, T, V, W, and Y.
 59. The library ofclaim 57, wherein the light chain portion further comprises a pluralityof LC_(κ) CDR2 regions <1>AS<2>R<4><1> (SEQ ID NO:102), wherein <1> isan equimolar mixture of amino acid residues A, D, E, F, G, H, I, K, L,M, N, P, Q, R, S, T, V, W, and Y; <2> is 0.2 S and 0.044 of each of A,D, E, F, G, H, I, K, L, M, N, P, Q, R, T, V, W, and Y; and <4> is 0.2 Aand 0.044 each of D, E, F, G, H, I, K, L, M, N, P, Q, R, S, T, V, W, andY.
 60. The library of claim 57, wherein the LC_(κ) CDR1s (1) and (2) arepresent in the library in a ratio of 0.68:0.32.
 61. The library of claim56, wherein the LC_(κ) CDR3s (1), (2) and (3) are present in the libraryin a ratio of 0.65:0.1:0.25.
 62. The library of claim 54, wherein atleast a light chain portion of the collection are lambda light chains,each of which comprises a LC_(λ) CDR1 region, a LC_(λ) CDR2 region, anda LC_(λ) CDR3 region.
 63. The library of claim 62, wherein the lightchain portion further comprises a plurality of LC_(λ) CDR3 regionsselected from the group consisting of: (1) <4><5><4><2><4>S<4><4><4><4>V(SEQ ID NO:106), wherein <2> is 0.27 D, 0.27 N, and 0.027 each of A, E,F, G, H, I, K, L, M, P, Q, R, S, T, V, W, and Y; <4> is an equimolarmixture of amino acid residues A, D, E, F, G, H, I, K, L, M, N, P, Q, R,S, T, V, and W; and <5> is 0.36 S and 0.0355 each of A, D, E, F, G, H,I, K, L, M, N, P, Q, R, T, V, W, and Y; (2) <5>SY<1><5>S<5><1><4>V (SEQID NO:19), wherein <1> is an equimolar mixture of A, D, E, F, G, H, I,K, L, M, N, P, Q, R, S, T, V, W, and Y; and <4> and <5> are as definedin (1) above; and (3) a mixture of (1) and (2) set forth above.
 64. Thelibrary of claim 63, wherein the light chain portion further comprises aplurality of LC_(λ) CDR1 regions selected from the group consisting of:(1) TG<1>SS<2>VG<1><3><2><3>VS (SEQ ID NO:18), wherein <1> is 0.27 T,0.27 G and 0.027 each of A, D, E, F, H, I, K, L, M, N, P, Q, R, S, V, W,and Y, <2> is 0.27 D, 0.27 N and 0.027 each of A, E, F, G, H, I, K, L,M, P, Q, R, S, T, V, W, and Y, and <3> is 0.36 Y and 0.036 each of A, D,E, F, G, H, I, K, L, M, N, P, Q, R, S, T, V, and W; (2)G<2><4>L<4><4><4><3><4><4> (SEQ ID NO:104), wherein <2> is as defined in(1) above and <4> is an equimolar mixture of amino acid residues A, D,E, F, G, H, I, K, L, M, N, P, Q, R, S, T, V, W, and Y; and (3) a mixtureof (1) and (2) set forth above.
 65. The library of claim 63, wherein thelight chain portion further comprises a plurality of LC_(λ) CDR2 regions<4><4><4><2>RPS (SEQ ID NO:105), wherein <2> is 0.27 D, 0.27 N, and0.027 each of A, E, F, G, H, I, K, L, M, P, Q, R, S, T, V, W, and Y and<4> is an equimolar mixture of amino acid residues A, D, E, F, G, H, I,K, L, M, N, P, Q, R, S, T, V, and W.
 66. The library of claim 64,wherein the light chain portion further comprises a plurality of LC_(λ)CDR2 regions <4><4><4><2>RPS (SEQ ID NO:105), wherein <2> is 0.27 D,0.27 N, and 0.027 each of A, E, F, G, H, I, K, L, M, P, Q, R, S, T, V,W, and Y and <4> is an equimolar mixture of amino acid residues A, D, E,F, G, H, I, K, L, M, N, P, Q, R, S, T, V, and W.
 67. The library ofclaim 64, where the LC_(λ) CDR1s (1) and (2) are present in the libraryin a ratio of 0.67:0.33.
 68. The library of claim 63, wherein the LC_(λ)CDR3s (1) and (2) are present in the library in an equimolar mixture.69. The library of claim 44, wherein the library is a library ofvectors.
 70. The library of claim 69, wherein the vectors are yeastvectors.
 71. The library of claim 44, wherein the library is a libraryof genetic packages.
 72. The library of claim 71, wherein the geneticpackages are cells, spores, or viral particles.
 73. The library of claim72, wherein the genetic packages are phage particles or yeast cells. 74.The library of claim 73, wherein the genetic packages are yeast cells,which display the collection of antibody heavy chains encoded by thefirst set of variegated DNA molecules.
 75. The library of claim 54,wherein the library is a library of vectors.
 76. The library of claim75, wherein the vectors are yeast vectors.
 77. The library of claim 54,wherein the library is a library of genetic packages.
 78. The library ofclaim 77, wherein the genetic packages are cells, spores, or viralparticles.
 79. The library of claim 78, wherein the genetic packages arephage particles or yeast cells.
 80. The library of claim 79, wherein thegenetic packages are yeast cells, which display the collection ofantibody heavy chains encoded by the first set of variegated DNAmolecules, the collection of antibody light chains encoded by the secondset of variegated DNA molecules, or both.